| Yeast Systematic Name | Yeast Symbol | SGDID | Analog Name | Analog Description | EC | Organism | Disease | Structure | Uniprot | Human ID | Human Symbol | HHsearch Probability | HHsearch E_value | HHsearch P_value | HHsearch Score | Flag Disease related | Flag Homo sapiens | Flag Mus musculus | Flag Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YMR216C | SKY1 | SGDID:S000004829 | Camk1 |
Calcium/calmodulin-dependent protein kinase type 1 (EC 2.7.11.17) (CaM kinase I) (CaM-KI) (CaM kinase I alpha) (CaMKI-alpha) |
2.7.11.17 | Rattus norvegicus | 1a06_a | Q63450 | 99.60 | 6.70E-21 | 6.60E-25 | 196.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | cgd2_1960 |
cgd2_1960 |
2.7.11.24 | Cryptosporidium parvum | 3oz6_a | A3FQ79 | 98.40 | 8.50E-11 | 9.60E-15 | 118.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | cgd4_240 |
cgd4_240 |
Cryptosporidium parvum | 3eb0_a | A3FQN0 | 98.20 | 5.10E-10 | 5.60E-14 | 113.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | GL50803_008037 GL50803_8037 |
GL50803_008037 GL50803_8037 |
Giardia intestinalis | 3gbz_a | A8BZ95 | 98.00 | 2.70E-09 | 3.10E-13 | 104.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | BN1205_040370 TGVEG_207820 |
BN1205_040370 TGVEG_207820 |
2.7.11.24 | Toxoplasma gondii | 3rp9_a | B6KP12 | 98.80 | 3.60E-13 | 4.00E-17 | 139.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | STT7 MICPUN_107392 |
STT7 MICPUN_107392 |
Micromonas commoda | 4ix3_b | C1EBN1 | 98.00 | 2.40E-09 | 2.80E-13 | 102.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | LDBPK_100540 |
LDBPK_100540 |
2.7.11.24 | Leishmania donovani | 4o2z_a | E9BA99 | 97.90 | 5.30E-09 | 5.80E-13 | 105.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | LDBPK_331470 |
LDBPK_331470 |
Leishmania donovani | 4qny_a | E9BQ78 | 97.80 | 7.60E-09 | 8.60E-13 | 102.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | PTSG_10090 |
PTSG_10090 |
2.7.11.17 | Salpingoeca rosetta | 5ig1_b | F2UPG5 | 97.80 | 7.70E-09 | 8.50E-13 | 102.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | ROP5B ROP5 TGRH88_057710 |
ROP5B ROP5 TGRH88_057710 |
Toxoplasma gondii | 4lv5_a | F2YGR7 | 98.10 | 7.60E-10 | 8.40E-14 | 110.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | MGG_04943 |
MGG_04943 |
2.7.11.24 | Magnaporthe oryzae | 5z33_a | G4N374 | 98.70 | 3.10E-12 | 3.30E-16 | 133.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | ROP5C |
ROP5C |
Toxoplasma gondii | 4lv8_a | I6ZQR7 | 97.90 | 4.10E-09 | 4.70E-13 | 104.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | CDC7 CDC7L1 |
Cell division cycle 7-related protein kinase (CDC7-related kinase) (HsCdc7) (huCdc7) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Open-Angle Glaucoma,Glaucoma, Primary Open Angle,Masa Syndrome |
4f9b_a | O00311 | ENSG00000097046 | CDC7 | 98.20 | 3.60E-10 | 4.00E-14 | 112.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | PLK4 SAK STK18 |
Serine/threonine-protein kinase PLK4 (EC 2.7.11.21) (Polo-like kinase 4) (PLK-4) (Serine/threonine-protein kinase 18) (Serine/threonine-protein kinase Sak) |
2.7.11.21 | Homo sapiens | Congenital Nervous System Abnormality,Autosomal Recessive Chorioretinopathy-Microcephaly Syndrome,Colorectal Cancer,Microcephaly,Seckel Syndrome,Microcephaly And Chorioretinopathy, Autosomal Recessive, 2,Isolated Growth Hormone Deficiency,Primary Autosomal Recessive Microcephaly,Joubert Syndrome 1,Isolated Growth Hormone Deficiency, Type Ia |
4jxf_a | O00444 | ENSG00000142731 | PLK4 | 97.80 | 9.40E-09 | 1.10E-12 | 95.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CHEK1 CHK1 |
Serine/threonine-protein kinase Chk1 (EC 2.7.11.1) (CHK1 checkpoint homolog) (Cell cycle checkpoint kinase) (Checkpoint kinase-1) |
2.7.11.1 | Homo sapiens | Tongue Carcinoma,Neuroblastoma,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Cerebellar Disease,Ovarian Cancer,Breast Cancer,Colorectal Cancer,Microcephaly,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Retinoblastoma,Esophageal Cancer,Seckel Syndrome,Mantle Cell Lymphoma,Pigmentary Disorder, Reticulate, With Systemic Manifestations, X-Linked,Ovarian Clear Cell Carcinoma,Autosomal Recessive Cerebellar Ataxia,Li-Fraumeni Syndrome,Ataxia-Telangiectasia,Medulloblastoma,Primary Autosomal Recessive Microcephaly,Lung Cancer |
2e9v_b | O14757 | ENSG00000149554 | CHEK1 | 97.90 | 4.40E-09 | 5.20E-13 | 97.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | IKBKB IKKB |
Inhibitor of nuclear factor kappa-B kinase subunit beta (I-kappa-B-kinase beta) (IKK-B) (IKK-beta) (IkBKB) (EC 2.7.11.10) (I-kappa-B kinase 2) (IKK2) (Nuclear factor NF-kappa-B inhibitor kinase beta) (NFKBIKB) (Serine/threonine protein kinase IKBKB) (EC 2.7.11.1) |
2.7.11.1,2.7.11.10, | Homo sapiens | Non-Alcoholic Fatty Liver Disease,Bone Cancer,Diabetes Mellitus,Severe Combined Immunodeficiency Due To Ikk2 Deficiency,Alzheimer Disease,Ectodermal Dysplasia,T-Cell Lymphoblastic Leukemia/Lymphoma,Human Cytomegalovirus Infection,Hepatitis,Asbestos-Related Lung Carcinoma,Combined Immunodeficiency,Breast Cancer,Colorectal Cancer,Oral Candidiasis,Prostate Cancer,Immunodeficiency 15b,Body Mass Index Quantitative Trait Locus 11,Skin Disease,Type 2 Diabetes Mellitus,Immunodeficiency 15a,Inflammatory Bowel Disease,Tooth Agenesis,Tuberous Sclerosis 1,Immunodeficiency 45,Incontinentia Pigmenti,Kaposi Sarcoma,Autosomal Recessive Non-Syndromic Intellectual Disability,Lung Cancer,Pancreatic Cancer |
4kik_a | O14920 | ENSG00000104365 | IKBKB | 97.70 | 1.50E-08 | 1.30E-12 | 114.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CASK LIN2 |
Peripheral plasma membrane protein CASK (hCASK) (EC 2.7.11.1) (Calcium/calmodulin-dependent serine protein kinase) (Protein lin-2 homolog) |
2.7.11.1 | Homo sapiens | Cask-Related Disorders,Cerebellar Hypoplasia,Constipation,Congenital Nystagmus,Pathologic Nystagmus,Neurofibromatosis, Type I,Fraser Syndrome 1,Cask Disorders,Cerebellar Disease,Dystonia,Glucosephosphate Dehydrogenase Deficiency,Lobular Neoplasia,X-Linked Intellectual Disability, Najm Type,Cask-Related Intellectual Disability,Microcephaly,Hypertonia,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Fg Syndrome 4,Helsmoortel-Van Der Aa Syndrome,Aland Island Eye Disease,Developmental And Epileptic Encephalopathy 8,Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia,Anemia, Nonspherocytic Hemolytic, Due To G6pd Deficiency,Coffin-Siris Syndrome 1,Early Infantile Epileptic Encephalopathy,Opitz-Kaveggia Syndrome,Pontocerebellar Hypoplasia,Autism,Cerebellar Hypoplasia/Atrophy, Epilepsy, And Global Developmental Delay,Peho Syndrome |
3c0g_b | O14936 | ENSG00000147044 | CASK | 98.80 | 8.20E-13 | 9.00E-17 | 132.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | AURKA AIK AIRK1 ARK1 AURA AYK1 BTAK IAK1 STK15 STK6 |
Aurora kinase A (EC 2.7.11.1) (Aurora 2) (Aurora/IPL1-related kinase 1) (ARK-1) (Aurora-related kinase 1) (hARK1) (Breast tumor-amplified kinase) (Serine/threonine-protein kinase 15) (Serine/threonine-protein kinase 6) (Serine/threonine-protein kinase aurora-A) |
2.7.11.1 | Homo sapiens | Endometrial Cancer,Melanoma,Plasma Cell Neoplasm,Uterine Corpus Cancer,Atypical Teratoid Rhabdoid Tumor,Neuroblastoma,Childhood Malignant Schwannoma,Adult Malignant Schwannoma,Bladder Cancer,Laryngeal Squamous Cell Carcinoma,Tetraploidy,Ovarian Cancer,Prostate Neuroendocrine Neoplasm,Breast Cancer,Colorectal Cancer,Endometrial Serous Adenocarcinoma,Hepatocellular Carcinoma,Rhabdomyosarcoma,Gastric Cancer,Prostate Cancer,Cervical Cancer,Lynch Syndrome,Esophageal Cancer,Donohue Syndrome,Colorectal Adenocarcinoma,Myeloma, Multiple,Medulloblastoma,Primary Autosomal Recessive Microcephaly,Lung Cancer,Pancreatic Cancer |
3h10_a | O14965 | ENSG00000087586 | AURKA | 97.80 | 8.80E-09 | 1.00E-12 | 96.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | GAK |
Cyclin-G-associated kinase (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Parkinson Disease, Late-Onset,Cataract 8, Multiple Types,Postencephalitic Parkinson Disease,Parkinson Disease 15, Autosomal Recessive Early-Onset |
5y7z_a | O14976 | ENSG00000178950 | GAK | 98.30 | 1.10E-10 | 1.30E-14 | 111.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | DCLK1 DCAMKL1 DCDC3A KIAA0369 |
Serine/threonine-protein kinase DCLK1 (EC 2.7.11.1) (Doublecortin domain-containing protein 3A) (Doublecortin-like and CAM kinase-like 1) (Doublecortin-like kinase 1) |
2.7.11.1 | Homo sapiens | Zellweger Syndrome,Colorectal Cancer,Attention Deficit-Hyperactivity Disorder,Chemical Colitis,Band Heterotopia |
5jzj_b | O15075 | ENSG00000133083 | DCLK1 | 98.00 | 1.70E-09 | 2.00E-13 | 103.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MAPK13 PRKM13 SAPK4 |
Mitogen-activated protein kinase 13 (MAP kinase 13) (MAPK 13) (EC 2.7.11.24) (Mitogen-activated protein kinase p38 delta) (MAP kinase p38 delta) (Stress-activated protein kinase 4) |
2.7.11.24 | Homo sapiens | 3coi_a | O15264 | ENSG00000156711 | MAPK13 | 98.00 | 1.40E-09 | 1.60E-13 | 107.70 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR216C | SKY1 | SGDID:S000004829 | PDPK1 PDK1 |
3-phosphoinositide-dependent protein kinase 1 (hPDK1) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Endometrial Cancer,Noonan Syndrome 1,Esophageal Adenosquamous Carcinoma,Prostate Cancer,Tuberous Sclerosis 1,Lung Cancer |
1h1w_a | O15530 | ENSG00000140992 | PDPK1 | 97.90 | 5.30E-09 | 6.00E-13 | 99.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | ROP8 |
ROP8 |
Toxoplasma gondii | 3byv_a | O15693 | 97.90 | 5.00E-09 | 5.60E-13 | 105.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | DAPK3 ZIPK |
Death-associated protein kinase 3 (DAP kinase 3) (EC 2.7.11.1) (DAP-like kinase) (Dlk) (MYPT1 kinase) (Zipper-interacting protein kinase) (ZIP-kinase) |
2.7.11.1 | Homo sapiens | Recessive Dystrophic Epidermolysis Bullosa |
1yrp_a | O43293 | ENSG00000167657 | DAPK3 | 98.00 | 2.20E-09 | 2.50E-13 | 100.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | DYRK3 |
Dual specificity tyrosine-phosphorylation-regulated kinase 3 (EC 2.7.12.1) (Regulatory erythroid kinase) (REDK) |
2.7.12.1 | Homo sapiens | Fungal Meningitis,Neuroaspergillosis,Mental Retardation, Autosomal Dominant 7 |
5y86_a | O43781 | ENSG00000143479 | DYRK3 | 99.20 | 2.10E-15 | 2.10E-19 | 166.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | BIK1 At2g39660 F12L6.32 F17A14.3 |
Serine/threonine-protein kinase BIK1 (EC 2.7.11.1) (Protein BOTRYTIS-INDUCED KINASE 1) |
2.7.11.1 | Arabidopsis thaliana | 5tos_a | O48814 | 98.50 | 2.30E-11 | 2.50E-15 | 123.50 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | PBL2 APK2A KIN1 At1g14370 F14L17.14 |
Probable serine/threonine-protein kinase PBL2 (EC 2.7.11.1) (PBS1-like protein 2) (Protein kinase 2A) |
2.7.11.1 | Arabidopsis thaliana | 6j5t_d | O49839 | 98.70 | 1.90E-12 | 2.10E-16 | 133.30 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | unc-43 K11E8.1 |
Calcium/calmodulin-dependent protein kinase type II (CaM kinase II) (EC 2.7.11.17) (Uncoordinated protein 43) |
2.7.11.17 | Caenorhabditis elegans | 2bdw_b | O62305 | 97.80 | 1.20E-08 | 1.30E-12 | 102.00 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | ssp2 SPCC74.03c |
SNF1-like protein kinase ssp2 (EC 2.7.11.1) |
2.7.11.1 | Schizosaccharomyces pombe | 3h4j_b | O74536 | 97.80 | 1.10E-08 | 1.20E-12 | 100.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | ULK1 KIAA0722 |
Serine/threonine-protein kinase ULK1 (EC 2.7.11.1) (Autophagy-related protein 1 homolog) (ATG1) (hATG1) (Unc-51-like kinase 1) |
2.7.11.1 | Homo sapiens | Retinitis Pigmentosa,Alzheimer Disease,Amyotrophic Lateral Sclerosis 1,Tuberous Sclerosis 2,Acute Laryngopharyngitis,Tuberous Sclerosis 1,Huntington Disease |
4wno_a | O75385 | ENSG00000177169 | ULK1 | 97.80 | 6.70E-09 | 7.80E-13 | 98.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | ERN1 IRE1 |
Serine/threonine-protein kinase/endoribonuclease IRE1 (Endoplasmic reticulum-to-nucleus signaling 1) (Inositol-requiring protein 1) (hIRE1p) (Ire1-alpha) (IRE1a) [Includes: Serine/threonine-protein kinase (EC 2.7.11.1); Endoribonuclease (EC 3.1.26.-)] |
2.7.11.1 | Homo sapiens | Retinitis Pigmentosa,Non-Alcoholic Fatty Liver Disease,Prion Disease,Alzheimer Disease,Ovarian Cancer,Wolfram Syndrome,Epiphyseal Dysplasia, Multiple, With Early-Onset Diabetes Mellitus,Huntington Disease |
6hx1_a | O75460 | ENSG00000178607 | ERN1 | 98.00 | 2.20E-09 | 2.40E-13 | 109.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | RPS6KA5 MSK1 |
Ribosomal protein S6 kinase alpha-5 (S6K-alpha-5) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 5) (Nuclear mitogen- and stress-activated protein kinase 1) (RSK-like protein kinase) (RSKL) |
2.7.11.1 | Homo sapiens | Septic Myocarditis,Coffin-Lowry Syndrome |
3kn5_b | O75582 | ENSG00000100784 | RPS6KA5 | 97.80 | 8.30E-09 | 9.30E-13 | 100.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CDKL5 STK9 |
Cyclin-dependent kinase-like 5 (EC 2.7.11.22) (Serine/threonine-protein kinase 9) |
2.7.11.22 | Homo sapiens | Cdkl5 Deficiency Disorder,Ohtahara Syndrome,Seizure Disorder,Childhood Absence Epilepsy,Epilepsy,Gait Apraxia,Gene Duplication Disease,Nicolaides-Baraitser Syndrome,Amyotrophic Lateral Sclerosis 1,Angelman Syndrome,Focal Epilepsy,Developmental And Epileptic Encephalopathy 14,Epilepsy With Generalized Tonic-Clonic Seizures,Congenital Nervous System Abnormality,Developmental And Epileptic Encephalopathy,Fundus Dystrophy,Juvenile Retinoschisis,Bruxism,X-Linked Congenital Retinoschisis,Early Myoclonic Encephalopathy,Stxbp1 Encephalopathy,Microcephaly,Mental Retardation, Autosomal Dominant 20,Encephalopathy,Benign Neonatal Seizures,Alacrima, Achalasia, And Mental Retardation Syndrome,Benign Epilepsy With Centrotemporal Spikes,Developmental And Epileptic Encephalopathy 9,Methylmalonic Acidemia,Benign Familial Neonatal Epilepsy,West Syndrome,Disease Of Mental Health,Lubs X-Linked Mental Retardation Syndrome,Fragile X Syndrome,Pitt-Hopkins Syndrome,Mowat-Wilson Syndrome,Developmental And Epileptic Encephalopathy 2,Lennox-Gastaut Syndrome,Sturge-Weber Syndrome,Neonatal Period Electroclinical Syndrome,Infancy Electroclinical Syndrome,Childhood Electroclinical Syndrome,Early Infantile Epileptic Encephalopathy,Developmental And Epileptic Encephalopathy 4,Myasthenic Syndrome, Congenital, 11, Associated With Acetylcholine Receptor Deficiency,Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 1,Aicardi Syndrome,Specific Developmental Disorder,Pervasive Developmental Disorder,Dravet Syndrome,Developmental And Epileptic Encephalopathy 1,Benign Familial Infantile Epilepsy,Generalized Epilepsy With Febrile Seizures Plus,Pyruvate Dehydrogenase E1-Alpha Deficiency,Retinoschisis 1, X-Linked, Juvenile,Rett Syndrome,Epilepsy, Myoclonic Juvenile,Autism,Christianson Syndrome,Epilepsy, Idiopathic Generalized,Peho Syndrome |
4bgq_a | O76039 | ENSG00000008086 | CDKL5 | 98.30 | 1.70E-10 | 2.00E-14 | 109.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | STK17B DRAK2 |
Serine/threonine-protein kinase 17B (EC 2.7.11.1) (DAP kinase-related apoptosis-inducing protein kinase 2) |
2.7.11.1 | Homo sapiens | Colon Squamous Cell Carcinoma |
6qf4_a | O94768 | ENSG00000081320 | STK17B | 97.80 | 9.80E-09 | 1.10E-12 | 100.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MAP4K4 HGK KIAA0687 NIK |
Mitogen-activated protein kinase kinase kinase kinase 4 (EC 2.7.11.1) (HPK/GCK-like kinase HGK) (MAPK/ERK kinase kinase kinase 4) (MEK kinase kinase 4) (MEKKK 4) (Nck-interacting kinase) |
2.7.11.1 | Homo sapiens | Arteriovenous Malformations Of The Brain,Autosomal Recessive Distal Hereditary Motor Neuronopathy,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1,Theileriasis |
4u3y_a | O95819 | ENSG00000071054 | MAP4K4 | 98.60 | 8.00E-12 | 9.10E-16 | 122.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | PAK4 KIAA1142 |
Serine/threonine-protein kinase PAK 4 (EC 2.7.11.1) (p21-activated kinase 4) (PAK-4) |
2.7.11.1 | Homo sapiens | Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease |
4xbr_a | O96013 | ENSG00000130669 | PAK4 | 97.80 | 6.40E-09 | 7.00E-13 | 104.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CHEK2 CDS1 CHK2 RAD53 |
Serine/threonine-protein kinase Chk2 (EC 2.7.11.1) (CHK2 checkpoint homolog) (Cds1 homolog) (Hucds1) (hCds1) (Checkpoint kinase 2) |
2.7.11.1 | Homo sapiens | Squamous Cell Carcinoma,Cerebral Hemisphere Lipoma,Corpus Callosum Lipoma,Adenoid Cystic Carcinoma,Cowden Syndrome,Cervical Adenoma Malignum,Leiomyosarcoma,Bilateral Breast Cancer,B-Lymphoblastic Leukemia/Lymphoma,Diffuse Midline Glioma, H3 K27m-Mutant,Essential Thrombocythemia,Congenital Heart Defects, Multiple Types, 3,Familial Colorectal Cancer,Leukemia,Inherited Cancer-Predisposing Syndrome,Wilms Tumor 5,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Li-Fraumeni Syndrome 1,Telangiectasis,Basal Cell Carcinoma,Lung Leiomyosarcoma,Prostate Leiomyosarcoma,Cerebellar Disease,Bile Duct Cystadenoma,T-Cell Prolymphocytic Leukemia,Nk-Cell Enteropathy,Ovarian Cancer,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Colorectal Cancer,Li-Fraumeni Syndrome 2,Premature Menopause,Rhabdomyosarcoma,Xeroderma Pigmentosum, Variant Type,Sarcoma,Fanconi Anemia, Complementation Group A,Bone Osteosarcoma,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Thrombocytopenia,Lynch Syndrome,Esophageal Cancer,Seckel Syndrome,Myelodysplastic Syndrome,Gastric Cancer, Hereditary Diffuse,Tumor Predisposition Syndrome,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Wilms Tumor 1,Autosomal Recessive Cerebellar Ataxia,Lymphoma,Nijmegen Breakage Syndrome,Colitis,Li-Fraumeni Syndrome,Premature Ovarian Failure 1,Ataxia-Telangiectasia,Melanoma, Cutaneous Malignant 1,Lung Cancer,Osteogenic Sarcoma |
3i6u_a | O96017 | ENSG00000183765 | CHEK2 | 98.60 | 5.40E-12 | 5.80E-16 | 130.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | pk7 |
pk7 |
Plasmodium falciparum | 2pml_x | O96214 | 98.70 | 1.50E-12 | 1.70E-16 | 130.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | PHKG1 PHKG |
Phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform (EC 2.7.11.19) (Phosphorylase kinase subunit gamma-1) (Serine/threonine-protein kinase PHKG1) (EC 2.7.11.1) (EC 2.7.11.26) |
2.7.11.1,2.7.11.19,2.7.11.26 | Oryctolagus cuniculus | 2phk_a | P00518 | 97.80 | 8.10E-09 | 9.50E-13 | 96.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | ABL1 ABL JTK7 |
Tyrosine-protein kinase ABL1 (EC 2.7.10.2) (Abelson murine leukemia viral oncogene homolog 1) (Abelson tyrosine-protein kinase 1) (Proto-oncogene c-Abl) (p150) |
2.7.10.2 | Homo sapiens | Heart Disease,Childhood Acute Lymphocytic Leukemia,Childhood T-Cell Acute Lymphoblastic Leukemia,Myeloid And Lymphoid Neoplasms Associated With Pdgfra Rearrangement,Chronic Neutrophilic Leukemia,Melanoma,Chronic Eosinophilic Leukemia,Leukemia, Chronic Myeloid,B-Lymphoblastic Leukemia/Lymphoma,B-Lymphoblastic Leukemia/Lymphoma With Bcr-Abl1,B-Lymphoblastic Leukemia/Lymphoma With Hypodiploidy,B-Lymphoblastic Leukemia/Lymphoma, Bcr-Abl1-Like,B-Lymphoblastic Leukemia/Lymphoma With Iamp21,Lung Large Cell Carcinoma,Blood Platelet Disease,Essential Thrombocythemia,Myeloproliferative Neoplasm,Testicular Leukemia,Philadelphia-Negative Chronic Myeloid Leukemia,Leukemia,Mixed Phenotype Acute Leukemia,Myelophthisic Anemia,Blood Coagulation Disease,Hypereosinophilic Syndrome,Childhood Leukemia,Leukemia, Acute Myeloid,Bone Marrow Cancer,Myelodysplastic/Myeloproliferative Neoplasm,Hematologic Cancer,Leukemia, Acute Lymphoblastic,Moyamoya Angiopathy,Polycythemia,Leiomyomatosis,Central Nervous System Leukemia,Precursor T-Cell Acute Lymphoblastic Leukemia,Acquired Polycythemia,T-Cell Prolymphocytic Leukemia,Chronic Leukemia,Cockayne Syndrome,Prolymphocytic Leukemia,Lip And Oral Cavity Cancer,Ovarian Cancer,Myeloid Leukemia,T-Cell Acute Lymphoblastic Leukemia,Adult Acute Lymphocytic Leukemia,Breast Cancer,Colorectal Cancer,Congenital Heart Defects And Skeletal Malformations Syndrome,Deficiency Anemia,Leukemia, Acute Lymphoblastic 3,Retinoblastoma,Mental Retardation, Autosomal Dominant 29,Myelodysplastic Syndrome,Mental Retardation, Autosomal Dominant 33,Gastrointestinal Stromal Tumor,Lymphoblastic Leukemia, Acute, With Lymphomatous Features,Wilms Tumor 1,Leukemia, Chronic Lymphocytic,Dermatofibrosarcoma Protuberans,Ataxia-Telangiectasia,B-Cell Adult Acute Lymphocytic Leukemia,Atypical Chronic Myeloid Leukemia,Polycythemia Vera |
2f4j_a | P00519 | ENSG00000097007 | ABL1 | 98.10 | 5.70E-10 | 6.60E-14 | 105.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | EGFR ERBB ERBB1 HER1 |
Epidermal growth factor receptor (EC 2.7.10.1) (Proto-oncogene c-ErbB-1) (Receptor tyrosine-protein kinase erbB-1) |
2.7.10.1 | Homo sapiens | Esophageal Disease,Benign Breast Adenomyoepithelioma,Pancreatic Adenocarcinoma,Supratentorial Cancer,Skin Melanoma,Gliomatosis Cerebri,Uterine Body Mixed Cancer,Nail Disease,Uterine Carcinosarcoma,Endometrial Cancer,Epithelioid Sarcoma,Autosomal Dominant Polycystic Kidney Disease,Spinal Chordoma,Peritoneum Cancer,Allergic Cutaneous Vasculitis,Squamous Cell Carcinoma,Inflammatory Breast Carcinoma,Retinitis Pigmentosa,Brain Stem Glioma,Thyroid Gland Cancer,Hair Disease,Peritoneal Mesothelioma,Lung Cancer Susceptibility 3,Sebaceous Gland Disease,Penile Cancer,Adenoid Cystic Carcinoma,Carcinosarcoma,Submandibular Gland Cancer,Chordoma,Bone Cancer,Cowden Syndrome,Signet Ring Lung Adenocarcinoma,Polycystic Kidney Disease,Hepatitis C,Suppression Of Tumorigenicity 12,Melanoma,Leukemia, Chronic Myeloid,Gastroesophageal Adenocarcinoma,Lung Non-Squamous Non-Small Cell Carcinoma,Thyroid Gland Anaplastic Carcinoma,Diabetes Mellitus,Cowden Syndrome 1,Primary Peritoneal Carcinoma,Malignant Peritoneal Mesothelioma,Papillary Squamous Carcinoma,Cholecystitis,Acneiform Dermatitis,Covid-19,Rectum Adenocarcinoma,Synchronous Bilateral Breast Carcinoma,Peripheral Nervous System Neoplasm,Uterine Corpus Cancer,Connective Tissue Cancer,Drug-Induced Hepatitis,Frontal Lobe Neoplasm,Clear Cell Renal Cell Carcinoma,Vulvar Disease,Rasopathy,Vulva Squamous Cell Carcinoma,Acth-Secreting Pituitary Adenoma,Mucoepidermoid Carcinoma,Large Cell Carcinoma,Keratosis Pilaris Atrophicans Faciei,Neurofibroma,Esophageal Basaloid Squamous Cell Carcinoma,Bile Duct Cancer,Intestinal Benign Neoplasm,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,Oral Cancer,Orbital Lymphangioma,Doxorubicin Induced Cardiomyopathy,Mammary Analogue Secretory Carcinoma,Amelogenesis Imperfecta,Human Cytomegalovirus Infection,Retinal Cancer,Biliary Tract Disease,Breast Metaplastic Carcinoma,Myeloproliferative Neoplasm,Differentiated Thyroid Carcinoma,Glial Tumor,Hepatitis,Infratentorial Cancer,Malignant Pleural Mesothelioma,Pulmonary Blastoma,Neurofibromatosis, Type I,Breast Scirrhous Carcinoma,Asbestos-Related Lung Carcinoma,Colon Adenocarcinoma,Adenosquamous Lung Carcinoma,Vulva Cancer,Adenosquamous Carcinoma,Neuroblastoma,Colonic Benign Neoplasm,Diffuse Astrocytoma,Bile Duct Adenocarcinoma,Esophagus Adenocarcinoma,Arteriovenous Malformations Of The Brain,Inherited Cancer-Predisposing Syndrome,Bronchiolo-Alveolar Adenocarcinoma,Intrahepatic Cholangiocarcinoma,Tubular Adenocarcinoma,Apocrine Adenocarcinoma,Adenocarcinoma In Situ,Gastroesophageal Junction Adenocarcinoma,Glioma,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Trachea Leiomyoma,Bone Marrow Cancer,Periampullary Adenocarcinoma,Recurrent Respiratory Papillomatosis,Basal Cell Carcinoma,Cataract,High Grade Ependymoma,Mixed Glioma,Larynx Cancer,Laryngeal Benign Neoplasm,Rectal Disease,Papilloma,Horseshoe Kidney,Autonomic Nervous System Neoplasm,Kidney Cancer,Dilated Cardiomyopathy,Gastroesophageal Reflux,Pleural Cancer,Basal Cell Nevus Syndrome,Transitional Cell Carcinoma,Myoma,Hemangioblastoma,Bladder Cancer,Paronychia,Lung Disease,Ethmoid Sinus Adenocarcinoma,Soft Tissue Sarcoma,Thymus Gland Disease,Brain Cancer,Colonic Disease,Acute Interstitial Pneumonia,Hypopharynx Cancer,Mixed Cell Adenoma,Lung Adenoma,Diarrhea,Endometrial Adenocarcinoma,Laryngeal Squamous Cell Carcinoma,Oropharynx Cancer,Cervix Carcinoma,Oral Cavity Cancer,Keratinizing Squamous Cell Carcinoma,Basaloid Squamous Cell Carcinoma,Lip And Oral Cavity Cancer,Ovarian Cancer,Neonatal Inflammatory Skin And Bowel Disease,Supraglottis Cancer,Adenocarcinoma,In Situ Carcinoma,Testicular Cancer,Breast Ductal Carcinoma,Breast Malignant Phyllodes Tumor,Charcot-Marie-Tooth Disease,Mucinous Adenocarcinoma,Cervical Adenosquamous Carcinoma,Breast Carcinoma In Situ,Lung Carcinoma In Situ,Lymphoepithelioma-Like Carcinoma,Breast Cancer,Pleomorphic Carcinoma,Glioblastoma,Tonsil Cancer,Squamous Cell Carcinoma, Head And Neck,Malignant Astrocytoma,High Grade Glioma,Gliosarcoma,Giant Cell Glioblastoma,Anaplastic Astrocytoma,Colorectal Cancer,Interstitial Lung Disease,Peripheral Nervous System Disease,Nervous System Cancer,Familial Hypercholesterolemia,Squamous Blepharitis,Gallbladder Cancer,Hepatocellular Carcinoma,Anus Disease,Keratoacanthoma,Skin Papilloma,Inverted Papilloma,Salivary Gland Disease,Oligodendroglioma,Spinal Cord Oligodendroglioma,Malignant Peripheral Nerve Sheath Tumor,Microglandular Adenosis,Anus Cancer,Toxic Shock Syndrome,Tooth Disease,Rhabdomyosarcoma,Hepatitis C Virus,Biliary Tract Cancer,Tongue Disease,Thymoma,Thymus Cancer,Thymic Carcinoma,Prostatic Hypertrophy,Peutz-Jeghers Syndrome,Immunodeficiency 54,Mammary Paget'S Disease,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Lymphangioma,Prostate Cancer,Disease Of Mental Health,Pancreatic Ductal Adenocarcinoma,Cholangiocarcinoma,Gallbladder Adenocarcinoma,Cerebral Ventricle Cancer,Pancreatic Ductal Carcinoma,Placental Site Trophoblastic Tumor,Ovarian Cystadenocarcinoma,Penile Disease,Pleural Disease,Mixed Cell Type Cancer,Central Nervous System Cancer,Respiratory System Disease,Cerebrum Cancer,Lung Benign Neoplasm,Integumentary System Disease,Skin Disease,Cervical Adenocarcinoma,Ovary Adenocarcinoma,Verrucous Carcinoma,Cervical Squamous Cell Carcinoma,Esophagus Verrucous Carcinoma,Childhood Medulloblastoma,Lynch Syndrome,Lung Squamous Cell Carcinoma,Hypotrichosis 13,Thyroid Gland Follicular Carcinoma,Renal Cell Carcinoma, Papillary, 1,Small Cell Cancer Of The Lung,Exanthem,Inflammatory Skin And Bowel Disease, Neonatal, 2,Esophageal Cancer,Respiratory System Benign Neoplasm,Gastrointestinal System Benign Neoplasm,Alveolar Soft Part Sarcoma,Small Cell Carcinoma,Tumor Predisposition Syndrome,Ewing Sarcoma,Lymphangioleiomyomatosis,Gastrointestinal Stromal Tumor,Colorectal Adenocarcinoma,Tongue Squamous Cell Carcinoma,Oral Squamous Cell Carcinoma,Pulmonary Adenocarcinoma In Situ,Large Cell Neuroendocrine Carcinoma,Bone Squamous Cell Carcinoma,Salivary Gland Carcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Renal Cell Carcinoma, Nonpapillary,Nasopharyngeal Carcinoma,Hypertension, Essential,Meningioma, Familial,Lymphoma,Pre-Malignant Neoplasm,Ductal Carcinoma In Situ,Estrogen-Receptor Positive Breast Cancer,Estrogen-Receptor Negative Breast Cancer,Progesterone-Receptor Negative Breast Cancer,Breast Benign Neoplasm,Cell Type Benign Neoplasm,Thoracic Benign Neoplasm,Brain Glioma,Pharynx Cancer,Gallbladder Disease,Leukemia, Chronic Lymphocytic,Amelogenesis Imperfecta, Type Ig,Li-Fraumeni Syndrome,Myeloma, Multiple,Medulloblastoma,Hepatoid Adenocarcinoma,Spinal Disease,Melanoma, Uveal,Retinitis Pigmentosa 11,Lung Cancer,Helicobacter Pylori Infection,Pancreatic Cancer |
5gnk_a | P00533 | ENSG00000146648 | EGFR | 98.20 | 4.10E-10 | 4.80E-14 | 106.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CDK1 CDC2 CDC28A CDKN1 P34CDC2 |
Cyclin-dependent kinase 1 (CDK1) (EC 2.7.11.22) (EC 2.7.11.23) (Cell division control protein 2 homolog) (Cell division protein kinase 1) (p34 protein kinase) |
2.7.11.22,2.7.11.23, | Homo sapiens | Bartholin'S Gland Adenocarcinoma,Bone Cancer,Polyploidy,Alzheimer Disease,Retinal Cancer,Neuroblastoma,Leukemia, Acute Myeloid,Hereditary Spastic Paraplegia,Leukemia, Acute Lymphoblastic,Bladder Cancer,Brain Cancer,Ovarian Cancer,Breast Cancer,Colorectal Cancer,Hepatocellular Carcinoma,Western Equine Encephalitis,Rhabdomyosarcoma,Fanconi Anemia, Complementation Group A,Neuronal Ceroid Lipofuscinosis,Breast Adenocarcinoma,Prostate Cancer,Cervical Cancer,Retinoblastoma,Lymphoma, Non-Hodgkin, Familial,Esophageal Cancer,Seckel Syndrome,Trichothiodystrophy 5, Nonphotosensitive,Mantle Cell Lymphoma,Gastrointestinal Stromal Tumor,Acute Promyelocytic Leukemia,Leukemia, Chronic Lymphocytic,Ceroid Lipofuscinosis, Neuronal, 2,Bloom Syndrome,Primary Autosomal Recessive Microcephaly,Ceroid Lipofuscinosis, Neuronal, 1,Lung Cancer,Frontotemporal Dementia |
4yc3_a | P06493 | ENSG00000170312 | CDK1 | 97.80 | 9.50E-09 | 1.10E-12 | 98.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MET |
Hepatocyte growth factor receptor (HGF receptor) (EC 2.7.10.1) (HGF/SF receptor) (Proto-oncogene c-Met) (Scatter factor receptor) (SF receptor) (Tyrosine-protein kinase Met) |
2.7.10.1 | Homo sapiens | Pancreatic Adenocarcinoma,Mesothelioma, Malignant,Skin Melanoma,Familial Renal Papillary Carcinoma,Spinal Chordoma,Follicular Adenoma,Thyroid Gland Cancer,Peritoneal Mesothelioma,Lung Cancer Susceptibility 3,Occipital Lobe Neoplasm,Mucositis,Acral Lentiginous Melanoma,Chondrosarcoma,Chordoma,Chronic Erosive Gastritis,Melanoma,Gastroesophageal Adenocarcinoma,Thyroid Gland Anaplastic Carcinoma,Dedifferentiated Liposarcoma,Myxofibrosarcoma,Tongue Carcinoma,Hereditary Renal Cell Carcinoma,Clear Cell Renal Cell Carcinoma,Hepatoblastoma,Bile Duct Cancer,Tall Cell Variant Papillary Carcinoma,Doxorubicin Induced Cardiomyopathy,Differentiated Thyroid Carcinoma,Malignant Pleural Mesothelioma,Refractive Error,Ependymoblastoma,Neuroblastoma,Inherited Cancer-Predisposing Syndrome,Arthrogryposis, Distal, Type 1a,Glioma,Kidney Cancer,Lung Disease,Ovarian Clear Cell Adenocarcinoma,Hypopharynx Cancer,Ovarian Cancer,Adenocarcinoma,Breast Ductal Carcinoma,Breast Carcinoma In Situ,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,High Grade Glioma,Colorectal Cancer,Papillary Carcinoma,Hepatocellular Carcinoma,Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb,Malignant Peripheral Nerve Sheath Tumor,Rhabdomyosarcoma,Biliary Tract Cancer,Gastric Cancer,Prostate Cancer,Papillary Thyroid Microcarcinoma,Cholangiocarcinoma,Microvascular Complications Of Diabetes 1,Lung Benign Neoplasm,Large Cell Medulloblastoma,Thyroid Gland Follicular Carcinoma,Autism 9,Renal Cell Carcinoma, Papillary, 1,Sarcoma, Synovial,Familial Mediterranean Fever, Autosomal Dominant,Barrett Esophagus,Distal Arthrogryposis,Alveolar Soft Part Sarcoma,Tumor Predisposition Syndrome,Vitreoretinopathy, Neovascular Inflammatory,Von Hippel-Lindau Syndrome,Salivary Gland Carcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Renal Cell Carcinoma, Nonpapillary,Autism Spectrum Disorder,Osteofibrous Dysplasia,Deafness, Autosomal Recessive 97,Inguinal Hernia,Medulloblastoma,Autism,Melanoma, Uveal,Pediatric Hepatocellular Carcinoma,Lung Cancer,Helicobacter Pylori Infection,Pancreatic Cancer |
4r1v_a | P08581 | ENSG00000105976 | MET | 98.10 | 8.50E-10 | 9.80E-14 | 104.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | PIM1 |
Serine/threonine-protein kinase pim-1 (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Retinitis Pigmentosa,Polyploidy,Plasma Protein Metabolism Disease,Primary Central Nervous System Lymphoma,Diamond-Blackfan Anemia,Myeloid Leukemia,Prostate Cancer,Mantle Cell Lymphoma |
1xr1_a | P11309 | ENSG00000137193 | PIM1 | 97.80 | 9.20E-09 | 1.10E-12 | 98.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CDK4 |
Cyclin-dependent kinase 4 (EC 2.7.11.22) (Cell division protein kinase 4) (PSK-J3) |
2.7.11.22 | Homo sapiens | Melanoma In Congenital Melanocytic Nevus,Pancreatic Adenocarcinoma,Skin Melanoma,Endometrial Cancer,Malignant Inflammatory Fibrous Histiocytoma,Childhood Acute Lymphocytic Leukemia,Retinitis Pigmentosa,Pancreas Sarcoma,Lung Cancer Susceptibility 3,Chondrosarcoma,Myofibrillar Myopathy,Rhabdomyosarcoma 2,Malignant Fibrous Histiocytoma,Melanoma,Plasma Cell Neoplasm,Dedifferentiated Liposarcoma,Myxofibrosarcoma,Myositis Ossificans,Leiomyosarcoma,Connective Tissue Cancer,Bone Sarcoma,Undifferentiated Embryonal Sarcoma Of The Liver,Infiltrating Lipoma,Large Cell Carcinoma,Ischemic Fasciitis,B-Cell Lymphoma,T-Cell Lymphoblastic Leukemia/Lymphoma,Ocular Cancer,Retinal Cancer,Familial Retinoblastoma,Embryonal Sarcoma,Retroperitoneal Sarcoma,Retroperitoneum Carcinoma,Neuroblastoma,Pilocytic Astrocytoma,Inherited Cancer-Predisposing Syndrome,Glioma,Leukemia, Acute Myeloid,Leukemia, Acute Lymphoblastic,Hereditary Melanoma,Ring Chromosome 7,Nodular Malignant Melanoma,Bladder Cancer,Spindle Cell Lipoma,Pleomorphic Lipoma,Lipoma Of Spermatic Cord,Paratesticular Lipoma,Melanoma, Cutaneous Malignant 3,Ring Chromosome,Lipoblastoma,Ovarian Cancer,Myeloid Leukemia,Burkitt Lymphoma,Adenocarcinoma,Testicular Cancer,T-Cell Acute Lymphoblastic Leukemia,Eye Disease,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Well-Differentiated Liposarcoma,Malignant Astrocytoma,Cellular Myxoid Liposarcoma,High Grade Glioma,Adult Liposarcoma,Pediatric Liposarcoma,Gliosarcoma,Gastric Liposarcoma,Breast Liposarcoma,Pleomorphic Liposarcoma,Mixed Liposarcoma,Spindle Cell Liposarcoma,Mediastinum Liposarcoma,Anaplastic Astrocytoma,Colorectal Cancer,Peripheral Nervous System Disease,Nervous System Cancer,Hepatocellular Carcinoma,Oligodendroglioma,Malignant Peripheral Nerve Sheath Tumor,Pheochromocytoma,Embryonal Rhabdomyosarcoma,Rhabdomyosarcoma,Myxoid Liposarcoma,Sarcoma,Extraosseous Osteosarcoma,Juxtacortical Osteosarcoma,Peripheral Osteosarcoma,Bone Osteosarcoma,Conventional Central Osteosarcoma,Liposarcoma Of Bone,Liposarcoma,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Infiltrating Angiolipoma,Thrombocytopenia,Retinoblastoma,Type 2 Diabetes Mellitus,Lung Squamous Cell Carcinoma,Diffuse Lipomatosis,Sensory System Disease,Muscle Cancer,Esophageal Cancer,Tumor Predisposition Syndrome,Diffuse Large B-Cell Lymphoma,Ewing Sarcoma,Mantle Cell Lymphoma,Acute Promyelocytic Leukemia,Inflammatory Myofibroblastic Tumor,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Nasopharyngeal Carcinoma,Lymphoma,Connective Tissue Benign Neoplasm,Kaposi Sarcoma,Leukemia, Chronic Lymphocytic,Li-Fraumeni Syndrome,Lipomatosis, Multiple,Dermatofibrosarcoma Protuberans,Parameningeal Embryonal Rhabdomyosarcoma,Myeloma, Multiple,Medulloblastoma,Melanoma, Cutaneous Malignant 1,Melanoma, Uveal,Neu-Laxova Syndrome 1,Lung Cancer,Osteogenic Sarcoma,Pancreatic Cancer |
2w99_b | P11802 | ENSG00000135446 | CDK4 | 97.90 | 2.80E-09 | 3.20E-13 | 102.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | GCN2 AAS1 YDR283C |
eIF-2-alpha kinase GCN2 (EC 2.7.11.1) (General control non-derepressible protein 2) (Serine/threonine-protein kinase GCN2) |
2.7.11.1 | Saccharomyces cerevisiae | 1zxe_c | P15442 | 98.50 | 1.90E-11 | 2.20E-15 | 116.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | PHKG2 |
Phosphorylase b kinase gamma catalytic chain, liver/testis isoform (PHK-gamma-LT) (PHK-gamma-T) (EC 2.7.11.19) (PSK-C3) (Phosphorylase kinase subunit gamma-2) |
2.7.11.19 | Homo sapiens | Glycogen Storage Disease Ixa,Glycogen Storage Disease Ixc,Glycogen Storage Disease,Phosphorylase Kinase Deficiency,Glycogen Storage Disease Due To Liver Phosphorylase Kinase Deficiency,Glycogen Storage Disease Ia,Glycogen Storage Disease, Type Ixd,Glycogen Storage Disease Ix,Glycogen Storage Disease Ixb |
2y7j_c | P15735 | ENSG00000156873 | PHKG2 | 97.80 | 6.50E-09 | 7.30E-13 | 103.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CKA1 YIL035C |
Casein kinase II subunit alpha (CK II subunit alpha) (EC 2.7.11.1) |
2.7.11.1 | Saccharomyces cerevisiae | 4fi1_a | P15790 | 97.90 | 3.30E-09 | 3.70E-13 | 106.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | PHO85 SSG3 YPL031C P7102.18A |
Cyclin-dependent protein kinase PHO85 (EC 2.7.11.22) (Negative regulator of the PHO system) (Serine/threonine-protein kinase PHO85) |
2.7.11.22 | Saccharomyces cerevisiae | 4krc_a | P17157 | 97.80 | 6.60E-09 | 7.40E-13 | 101.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | PRKACA PKACA |
cAMP-dependent protein kinase catalytic subunit alpha (PKA C-alpha) (EC 2.7.11.11) |
2.7.11.11 | Homo sapiens | Mixed Fibrolamellar Hepatocellular Carcinoma,Fibrolamellar Carcinoma,Cardioacrofacial Dysplasia 1,Dilated Cardiomyopathy,Acth-Independent Cushing Syndrome,Osteoporosis,Breast Cancer,Pigmented Nodular Adrenocortical Disease, Primary, 4,Primary Pigmented Nodular Adrenocortical Disease |
3ama_a | P17612 | ENSG00000072062 | PRKACA | 97.80 | 6.00E-09 | 6.70E-13 | 103.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | Rps6ka3 Mapkapk1b Rps6ka-rs1 Rsk2 |
Ribosomal protein S6 kinase alpha-3 (S6K-alpha-3) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 3) (p90-RSK 3) (p90RSK3) (MAP kinase-activated protein kinase 1b) (MAPK-activated protein kinase 1b) (MAPKAP kinase 1b) (MAPKAPK-1b) (Ribosomal S6 kinase 2) (RSK-2) (pp90RSK2) |
2.7.11.1 | Mus musculus | 5o1s_a | P18654 | 98.00 | 2.70E-09 | 2.90E-13 | 107.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | CSNK2A2 CK2A2 |
Casein kinase II subunit alpha' (CK II alpha') (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Connective Tissue Disease,Neonatal Leukemia,Distal Muscular Dystrophy With Anterior Tibial Onset,Spermatogenic Failure 50,Breast Adenocarcinoma,Theileriasis,Spermatogenic Failure 9 |
6hmq_a | P19784 | ENSG00000070770 | CSNK2A2 | 98.80 | 5.50E-13 | 6.00E-17 | 134.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | RAD53 MEC2 SAD1 SPK1 YPL153C P2588 |
Serine/threonine-protein kinase RAD53 (EC 2.7.12.1) (CHEK2 homolog) (Serine-protein kinase 1) |
2.7.12.1 | Saccharomyces cerevisiae | 4pdp_a | P22216 | 97.80 | 7.80E-09 | 8.80E-13 | 102.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | RPS6KB1 STK14A |
Ribosomal protein S6 kinase beta-1 (S6K-beta-1) (S6K1) (EC 2.7.11.1) (70 kDa ribosomal protein S6 kinase 1) (P70S6K1) (p70-S6K 1) (Ribosomal protein S6 kinase I) (Serine/threonine-protein kinase 14A) (p70 ribosomal S6 kinase alpha) (p70 S6 kinase alpha) (p70 S6K-alpha) (p70 S6KA) |
2.7.11.1 | Homo sapiens | Mitral Valve Disease,Retinitis Pigmentosa,Cowden Syndrome,Pyriform Sinus Cancer,Cowden Syndrome 1,Placental Choriocarcinoma,Uterus Perivascular Epithelioid Cell Tumor,Subependymal Glioma,Benign Ependymoma,Leukemia, Acute Myeloid,Nephronophthisis,Kidney Angiomyolipoma,Aortic Disease,Skin Amelanotic Melanoma,Ovarian Cancer,Tuberous Sclerosis 2,Tuberous Sclerosis,Breast Cancer,Glioblastoma,Colorectal Cancer,Hepatocellular Carcinoma,Rhabdomyosarcoma,Acute Laryngopharyngitis,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Diamond-Blackfan Anemia 20,Esophageal Cancer,Muscle Hypertrophy,Mantle Cell Lymphoma,Tuberous Sclerosis 1,Lymphangioleiomyomatosis,Leukodystrophy, Hypomyelinating, 12,Lung Cancer,Palmoplantar Keratoderma, Bothnian Type,Pancreatic Cancer |
3wf7_a | P23443 | ENSG00000108443 | RPS6KB1 | 98.00 | 2.50E-09 | 2.80E-13 | 104.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | PRKCH PKCL PRKCL |
Protein kinase C eta type (EC 2.7.11.13) (PKC-L) (nPKC-eta) |
2.7.11.13 | Homo sapiens | Myofibrillar Myopathy,Amphetamine Abuse,Stroke, Ischemic,Glioblastoma |
3txo_a | P24723 | ENSG00000027075 | PRKCH | 97.90 | 3.20E-09 | 3.60E-13 | 105.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CDK2 CDKN2 |
Cyclin-dependent kinase 2 (EC 2.7.11.22) (Cell division protein kinase 2) (p33 protein kinase) |
2.7.11.22 | Homo sapiens | Pancreatic Adenocarcinoma,Endometrial Cancer,Smooth Muscle Tumor,Melanoma,Endometrial Hyperplasia,Leukemia, Chronic Myeloid,Leiomyosarcoma,Ocular Cancer,Retinal Cancer,Neuroblastoma,Leukemia, Acute Myeloid,Leukemia, Acute Lymphoblastic,Bladder Cancer,Lung Adenoma,Laryngeal Squamous Cell Carcinoma,Ovarian Cancer,Testicular Cancer,Eye Disease,Uterine Sarcoma,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Colorectal Cancer,Nervous System Cancer,Hepatocellular Carcinoma,Microcephaly,Pheochromocytoma,Skin Carcinoma,Gastric Cancer,Prostate Cancer,Cervical Cancer,Cecal Benign Neoplasm,Retinoblastoma,Sensory System Disease,Trichothiodystrophy 5, Nonphotosensitive,Mantle Cell Lymphoma,Gastrointestinal Stromal Tumor,Cecum Adenoma,Leukemia, Chronic Lymphocytic,Ataxia-Telangiectasia,Melanoma, Cutaneous Malignant 1,Lung Cancer,Pancreatic Cancer |
4i3z_c | P24941 | ENSG00000123374 | CDK2 | 97.80 | 8.90E-09 | 1.00E-12 | 97.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | ACVR2A ACVR2 |
Activin receptor type-2A (EC 2.7.11.30) (Activin receptor type IIA) (ACTR-IIA) (ACTRIIA) |
2.7.11.30 | Homo sapiens | Chondroma,Mbd5 Haploinsufficiency,Brachydactyly, Type A2,Synovial Chondromatosis,Pre-Eclampsia,Colorectal Cancer,Du Pan Syndrome,Fibrodysplasia Ossificans Progressiva,Multiple Synostoses Syndrome |
4asx_a | P27037 | ENSG00000121989 | ACVR2A | 98.20 | 2.70E-10 | 3.10E-14 | 109.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MARK3 CTAK1 EMK2 |
MAP/microtubule affinity-regulating kinase 3 (EC 2.7.11.1) (C-TAK1) (cTAK1) (Cdc25C-associated protein kinase 1) (ELKL motif kinase 2) (EMK-2) (Protein kinase STK10) (Ser/Thr protein kinase PAR-1) (Par-1a) (Serine/threonine-protein kinase p78) |
2.7.11.1 | Homo sapiens | Focal Epithelial Hyperplasia,Osteoporosis,Peutz-Jeghers Syndrome,Gaucher Disease, Type Iii,Visual Impairment And Progressive Phthisis Bulbi |
2qnj_b | P27448 | ENSG00000075413 | MARK3 | 97.80 | 6.00E-09 | 6.80E-13 | 101.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MAPK1 ERK2 PRKM1 PRKM2 |
Mitogen-activated protein kinase 1 (MAP kinase 1) (MAPK 1) (EC 2.7.11.24) (ERT1) (Extracellular signal-regulated kinase 2) (ERK-2) (MAP kinase isoform p42) (p42-MAPK) (Mitogen-activated protein kinase 2) (MAP kinase 2) (MAPK 2) |
2.7.11.24 | Homo sapiens | Pancreatic Adenocarcinoma,Heart Disease,Learning Disability,Endometrial Cancer,Autosomal Dominant Polycystic Kidney Disease,Differentiating Neuroblastoma,Squamous Cell Carcinoma,Vascular Disease,Lung Cancer Susceptibility 3,Spinal Cord Injury,Polycystic Kidney Disease,Melanoma,Leukemia, Chronic Myeloid,Thyroid Gland Anaplastic Carcinoma,Diabetes Mellitus,Noonan Syndrome 13,Alzheimer Disease,Rasopathy,Retrograde Amnesia,Bile Duct Cancer,Specific Learning Disability,Human Cytomegalovirus Infection,Hepatitis,Mesangial Proliferative Glomerulonephritis,Insulin-Like Growth Factor I,Neuroblastoma,Angioimmunoblastic T-Cell Lymphoma,Glioma,Noonan Syndrome 1,Dilated Cardiomyopathy,Bladder Cancer,Lung Adenoma,Pediculus Humanus Corporis Infestation,Cystic Kidney Disease,Ovarian Cancer,Myeloid Leukemia,Burkitt Lymphoma,Tuberous Sclerosis,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Microphthalmia,Colorectal Cancer,Hepatocellular Carcinoma,Cardiofaciocutaneous Syndrome 1,Microcephaly,Opioid Addiction,Pheochromocytoma,Rhabdomyosarcoma,Hepatitis C Virus,Alacrima, Achalasia, And Mental Retardation Syndrome,Mood Disorder,Esophagus Sarcoma,Sarcoma,Anhidrosis,Pertussis,Fibrosarcoma,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Disease Of Mental Health,Cholangiocarcinoma,Cervical Cancer,Bladder Squamous Cell Carcinoma,Fragile X Syndrome,Bladder Urothelial Carcinoma,Esophageal Cancer,Muscle Hypertrophy,Fibrodysplasia Ossificans Progressiva,Chromosome 22q11.2 Deletion Syndrome, Distal,Ewing Sarcoma,Heart, Malformation Of,Acute Promyelocytic Leukemia,Kaposi Sarcoma,Cardiomyopathy, Familial Hypertrophic, 25,Lung Cancer,Gordon Holmes Syndrome,Pancreatic Cancer |
4zzn_a | P28482 | ENSG00000100030 | MAPK1 | 97.90 | 4.60E-09 | 5.20E-13 | 103.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | ACK2 |
Casein kinase II subunit alpha (EC 2.7.11.1) (CK II) (CK2-alpha) |
2.7.11.1 | Zea mays | 4dgn_a | P28523 | 98.00 | 2.10E-09 | 2.40E-13 | 104.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | HRR25 YPL204W |
Casein kinase I homolog HRR25 (EC 2.7.11.1) |
2.7.11.1 | Saccharomyces cerevisiae | 5cyz_a | P29295 | 98.40 | 4.40E-11 | 4.90E-15 | 121.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | EPHA3 ETK ETK1 HEK TYRO4 |
Ephrin type-A receptor 3 (EC 2.7.10.1) (EPH-like kinase 4) (EK4) (hEK4) (HEK) (Human embryo kinase) (Tyrosine-protein kinase TYRO4) (Tyrosine-protein kinase receptor ETK1) (Eph-like tyrosine kinase 1) |
2.7.10.1 | Homo sapiens | Large Cell Carcinoma,Lung Large Cell Carcinoma,Cerebral Artery Occlusion,Adenocarcinoma,Breast Cancer,Beriberi,Parkinson Disease, Late-Onset,Colorectal Cancer,Thiamine Deficiency Disease,Tumoral Calcinosis, Hyperphosphatemic, Familial, 1,Wet Beriberi |
2qol_a | P29320 | ENSG00000044524 | EPHA3 | 98.10 | 8.10E-10 | 8.80E-14 | 111.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | AKT1 PKB RAC |
RAC-alpha serine/threonine-protein kinase (EC 2.7.11.1) (Protein kinase B) (PKB) (Protein kinase B alpha) (PKB alpha) (Proto-oncogene c-Akt) (RAC-PK-alpha) |
2.7.11.1 | Homo sapiens | Adult Hepatocellular Carcinoma,Breast Papillomatosis,Esophageal Disease,Pancreatic Adenocarcinoma,Muscular Disease,Skin Melanoma,Liver Disease,Mitral Valve Disease,Heart Disease,Neurofibromatosis, Type Ii,Endometrial Cancer,Bile Duct Disease,Spinal Chordoma,Hepatopulmonary Syndrome,Squamous Cell Carcinoma,Pfeiffer Syndrome,Glucose Metabolism Disease,Childhood T-Cell Acute Lymphoblastic Leukemia,Hyperglycemia,Retinitis Pigmentosa,Thyroid Gland Cancer,Hair Disease,Macroglobulinemia,Lung Cancer Susceptibility 3,Kagami-Ogata Syndrome,Adenoid Cystic Carcinoma,Non-Alcoholic Fatty Liver Disease,Chordoma,Cowden Syndrome,Polycystic Kidney Disease,Microvascular Complications Of Diabetes 5,Suppression Of Tumorigenicity 12,Melanoma,Connective Tissue Disease,Ocular Hypertension,Leukemia, Chronic Myeloid,Overnutrition,Inherited Metabolic Disorder,Thyroid Gland Anaplastic Carcinoma,Diabetes Mellitus,Adenoma,Spherocytosis, Type 5,Cowden Syndrome 1,Breast Juvenile Papillomatosis,Lipid Storage Disease,Peripheral Nervous System Neoplasm,Uterine Corpus Cancer,Connective Tissue Cancer,Bone Sarcoma,Hypertrophic Cardiomyopathy,Placental Choriocarcinoma,Leukocyte Disease,Clear Cell Renal Cell Carcinoma,Hyperostosis,Alzheimer Disease,Hepatoblastoma,Rasopathy,Nasopharyngeal Disease,Myocardial Infarction,Major Depressive Disorder,Bile Duct Cancer,Intestinal Benign Neoplasm,Stroke, Ischemic,Teeth Hard Tissue Disease,Amyotrophic Lateral Sclerosis 1,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,T-Cell Lymphoblastic Leukemia/Lymphoma,Ocular Cancer,Amelogenesis Imperfecta,Retinal Cancer,Blood Platelet Disease,Biliary Tract Disease,Congenital Lipomatous Overgrowth, Vascular Malformations, And Epidermal Nevi,Infratentorial Cancer,Leptin Deficiency Or Dysfunction,Lymphatic System Disease,Neurofibromatosis, Type I,Insulin-Like Growth Factor I,Neuroblastoma,Colonic Benign Neoplasm,Subependymal Glioma,Blood Coagulation Disease,Benign Ependymoma,Pilocytic Astrocytoma,Diffuse Astrocytoma,Childhood Leukemia,Bile Duct Adenocarcinoma,Hemangioma Of Lung,Nevus, Epidermal,Distal Muscular Dystrophy With Anterior Tibial Onset,Retinal Vascular Disease,Psychotic Disorder,Leukemia, Acute Myeloid,Noonan Syndrome 1,Bone Marrow Cancer,Leber Plus Disease,Hemangioma,Leukemia, Acute Lymphoblastic,Cataract,Combined Immunodeficiency,Liver Cirrhosis,Pancreas Disease,Papilloma,Cardiovascular System Disease,Autonomic Nervous System Neoplasm,Kidney Cancer,Pleural Cancer,Basal Cell Nevus Syndrome,Cowden Syndrome 6,Bladder Cancer,Focal Segmental Glomerulosclerosis,Epithelial-Myoepithelial Carcinoma,Thymus Gland Disease,Brain Cancer,Colonic Disease,Lung Adenoma,Lung Oat Cell Carcinoma,Endometrial Adenocarcinoma,Oropharynx Cancer,Cervix Carcinoma,Ulcerative Colitis,Nervous System Disease,Osteoporosis,Anal Squamous Cell Carcinoma,Ovarian Cancer,Adenocarcinoma,Tuberous Sclerosis 2,In Situ Carcinoma,Tuberous Sclerosis,T-Cell Acute Lymphoblastic Leukemia,Eye Disease,Acute Megakaryocytic Leukemia,Breast Carcinoma In Situ,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Malignant Astrocytoma,Gliosarcoma,Parkinson Disease, Late-Onset,Colorectal Cancer,Peripheral Nervous System Disease,Nervous System Cancer,Ovarian Serous Cystadenocarcinoma,Cystadenocarcinoma,Serous Cystadenocarcinoma,Gallbladder Cancer,Hepatocellular Carcinoma,Premature Menopause,Combined Hepatocellular Carcinoma And Cholangiocarcinoma,Skin Papilloma,Partial Third-Nerve Palsy,Neurilemmoma,Rhabdomyosarcoma,Ischemia,Tongue Disease,Chronic Granulomatous Disease,Thymoma,Thymus Cancer,Ovarian Disease,Noonan Syndrome With Multiple Lentigines,Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease,Teratoma,Bipolar Disorder,Macular Degeneration, Age-Related, 1,Immunodeficiency 14,Sarcoma,Bone Osteosarcoma,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Cone-Rod Dystrophy 2,Prostate Cancer,Disease Of Mental Health,Pancreatic Ductal Adenocarcinoma,Cholangiocarcinoma,Proteus Syndrome,Cervical Cancer,Toxic Encephalopathy,Ovarian Cystadenocarcinoma,Body Mass Index Quantitative Trait Locus 11,Penile Disease,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Central Nervous System Cancer,Pulmonary Fibrosis, Idiopathic,Congenital Myasthenic Syndrome,Retinitis Pigmentosa 47,Respiratory System Disease,Integumentary System Disease,Skin Disease,Cervical Adenocarcinoma,Ovary Adenocarcinoma,Gastric Adenocarcinoma,Type 2 Diabetes Mellitus,Plasmacytoma,Cervical Squamous Cell Carcinoma,Lynch Syndrome,Hidradenoma,Lung Squamous Cell Carcinoma,Fragile X Syndrome,Thyroid Gland Follicular Carcinoma,Schizophrenia,Sensory System Disease,Bladder Urothelial Carcinoma,Lymphoma, Non-Hodgkin, Familial,Skeletal Muscle Cancer,Muscle Cancer,Small Cell Cancer Of The Lung,Immunodeficiency 36,Hypotrichosis 1,Exanthem,Esophageal Cancer,Severe Congenital Neutropenia,Respiratory System Benign Neoplasm,Reproductive Organ Benign Neoplasm,Gastrointestinal System Benign Neoplasm,Immune Deficiency Disease,Myelodysplastic Syndrome,Meningioma, Radiation-Induced,Wiskott-Aldrich Syndrome,X-Linked Monogenic Disease,Autosomal Genetic Disease,Diffuse Large B-Cell Lymphoma,Ewing Sarcoma,Mantle Cell Lymphoma,Peripheral T-Cell Lymphoma,Tuberous Sclerosis 1,Hashimoto Thyroiditis,Gastrointestinal Stromal Tumor,Diabetic Encephalopathy,Tongue Squamous Cell Carcinoma,Oral Squamous Cell Carcinoma,Huntington Disease,Renal Cell Carcinoma, Nonpapillary,Nasopharyngeal Carcinoma,Hypertension, Essential,Meningioma, Familial,Pre-Malignant Neoplasm,Lymphatic System Cancer,Ductal Carcinoma In Situ,Estrogen-Receptor Positive Breast Cancer,Cell Type Benign Neoplasm,Cardiovascular Organ Benign Neoplasm,Uterine Benign Neoplasm,Acquired Metabolic Disease,Kaposi Sarcoma,Colitis,Klippel-Trenaunay-Weber Syndrome,Gallbladder Disease,Leukemia, Chronic Lymphocytic,Amelogenesis Imperfecta, Type Ig,Systemic Lupus Erythematosus,Pelizaeus-Merzbacher Disease,Rett Syndrome,Myeloma, Multiple,Medulloblastoma,Spinal Disease,Autism,Melanoma, Cutaneous Malignant 1,Melanoma, Uveal,Lymphoproliferative Syndrome,Lung Cancer,Palmoplantar Keratoderma, Bothnian Type,Oculoectodermal Syndrome,Osteogenic Sarcoma,Pancreatic Cancer |
4gv1_a | P31749 | ENSG00000142208 | AKT1 | 97.90 | 4.50E-09 | 5.00E-13 | 103.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | TTK MPS1 MPS1L1 |
Dual specificity protein kinase TTK (EC 2.7.12.1) (Phosphotyrosine picked threonine-protein kinase) (PYT) |
2.7.12.1 | Homo sapiens | Polyposis Syndrome, Hereditary Mixed, 1,Hereditary Mixed Polyposis Syndrome,Osteogenesis Imperfecta, Type Xvii,Lung Cancer,Mosaic Variegated Aneuploidy Syndrome 1,Pancreatic Cancer |
4js8_a | P33981 | ENSG00000112742 | TTK | 97.90 | 5.30E-09 | 6.30E-13 | 96.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | PAN3 ECM35 YKL025C |
PAN2-PAN3 deadenylation complex subunit PAN3 (PAB1P-dependent poly(A)-specific ribonuclease) (Poly(A)-nuclease deadenylation complex subunit 3) (PAN deadenylation complex subunit 3) |
Saccharomyces cerevisiae | 4xr7_l | P36102 | 98.10 | 9.40E-10 | 1.00E-13 | 115.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | MAP3K8 COT ESTF |
Mitogen-activated protein kinase kinase kinase 8 (EC 2.7.11.25) (Cancer Osaka thyroid oncogene) (Proto-oncogene c-Cot) (Serine/threonine-protein kinase cot) (Tumor progression locus 2) (TPL-2) |
2.7.11.25 | Homo sapiens | Indolent Plasma Cell Myeloma,Paronychia,Skin Lipoma,Rheumatoid Arthritis,Lung Cancer |
4y85_b | P41279 | ENSG00000107968 | MAP3K8 | 97.80 | 7.10E-09 | 8.00E-13 | 101.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MAPK8 JNK1 PRKM8 SAPK1 SAPK1C |
Mitogen-activated protein kinase 8 (MAP kinase 8) (MAPK 8) (EC 2.7.11.24) (JNK-46) (Stress-activated protein kinase 1c) (SAPK1c) (Stress-activated protein kinase JNK1) (c-Jun N-terminal kinase 1) |
2.7.11.24 | Homo sapiens | Liver Disease,Endometrial Cancer,Lung Cancer Susceptibility 3,Non-Alcoholic Fatty Liver Disease,Hepatitis C,Acantholytic Acanthoma,Leukemia, Chronic Myeloid,Diabetes Mellitus,Non-Alcoholic Steatohepatitis,Fatty Liver Disease,Alzheimer Disease,Epidermolysis Bullosa Simplex,Hepatitis,Colon Adenocarcinoma,Neuroblastoma,Cervical Non-Keratinizing Squamous Cell Carcinoma,Hereditary Spastic Paraplegia,Leukemia, Acute Lymphoblastic,Ovarian Cancer,Burkitt Lymphoma,Breast Cancer,Glioblastoma,Parkinson Disease, Late-Onset,Colorectal Cancer,Hepatocellular Carcinoma,Sarcoma,Fibrosarcoma,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Disease Of Mental Health,Rheumatoid Arthritis,Type 2 Diabetes Mellitus,Renal Fibrosis,Acute Promyelocytic Leukemia,Huntington Disease,Nasopharyngeal Carcinoma,Cardiomyopathy, Familial Hypertrophic, 25,Neu-Laxova Syndrome 1,Lung Cancer,Pancreatic Cancer |
2xrw_a | P45983 | ENSG00000107643 | MAPK8 | 99.20 | 2.10E-15 | 2.40E-19 | 153.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MAPK9 JNK2 PRKM9 SAPK1A |
Mitogen-activated protein kinase 9 (MAP kinase 9) (MAPK 9) (EC 2.7.11.24) (JNK-55) (Stress-activated protein kinase 1a) (SAPK1a) (Stress-activated protein kinase JNK2) (c-Jun N-terminal kinase 2) |
2.7.11.24 | Homo sapiens | Leukemia, Chronic Myeloid,Diabetes Mellitus,Alzheimer Disease,Nephronophthisis,Breast Cancer,Colorectal Cancer,Pheochromocytoma,Skin Carcinoma,Cardiomyopathy, Familial Hypertrophic, 25 |
3npc_a | P45984 | ENSG00000050748 | MAPK9 | 98.10 | 1.20E-09 | 1.40E-13 | 109.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MAP2K4 JNKK1 MEK4 MKK4 PRKMK4 SEK1 SERK1 SKK1 |
Dual specificity mitogen-activated protein kinase kinase 4 (MAP kinase kinase 4) (MAPKK 4) (EC 2.7.12.2) (JNK-activating kinase 1) (MAPK/ERK kinase 4) (MEK 4) (SAPK/ERK kinase 1) (SEK1) (Stress-activated protein kinase kinase 1) (SAPK kinase 1) (SAPKK-1) (SAPKK1) (c-Jun N-terminal kinase kinase 1) (JNKK) |
2.7.12.2 | Homo sapiens | Melanoma,Breast Mucoepidermoid Carcinoma,Anthrax Disease,Neuroblastoma,Hereditary Spastic Paraplegia,Ureteral Obstruction,Ovarian Cancer,Breast Cancer,Colorectal Cancer,Prostate Cancer,Ovarian Serous Carcinoma,Cardiomyopathy, Familial Hypertrophic, 25,Lung Cancer,Pancreatic Cancer |
3aln_a | P45985 | ENSG00000065559 | MAP2K4 | 97.70 | 1.30E-08 | 1.50E-12 | 98.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MAPKAPK2 |
MAP kinase-activated protein kinase 2 (MAPK-activated protein kinase 2) (MAPKAP kinase 2) (MAPKAP-K2) (MAPKAPK-2) (MK-2) (MK2) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Monocytic Leukemia,Tuberous Sclerosis 2,Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease |
3m2w_a | P49137 | ENSG00000162889 | MAPKAPK2 | 98.10 | 6.60E-10 | 7.40E-14 | 107.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CDK8 |
Cyclin-dependent kinase 8 (EC 2.7.11.22) (EC 2.7.11.23) (Cell division protein kinase 8) (Mediator complex subunit CDK8) (Mediator of RNA polymerase II transcription subunit CDK8) (Protein kinase K35) |
2.7.11.22,2.7.11.23, | Homo sapiens | Heart Disease,Ebstein Anomaly,Hydrocephalus, Congenital, 1,Reproductive Organ Benign Neoplasm,Heart, Malformation Of,Diaphragmatic Hernia, Congenital,Colorectal Adenocarcinoma,Intellectual Developmental Disorder With Hypotonia And Behavioral Abnormalities,Opitz-Kaveggia Syndrome,Breast Benign Neoplasm,Uterine Benign Neoplasm,Thoracic Benign Neoplasm |
5xs2_a | P49336 | ENSG00000132964 | CDK8 | 98.10 | 1.00E-09 | 1.10E-13 | 111.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CLK1 CLK |
Dual specificity protein kinase CLK1 (EC 2.7.12.1) (CDC-like kinase 1) |
2.7.12.1 | Homo sapiens | Pick Disease Of Brain |
6ft8_a | P49759 | ENSG00000013441 | CLK1 | 98.20 | 5.20E-10 | 6.10E-14 | 108.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CLK3 |
Dual specificity protein kinase CLK3 (EC 2.7.12.1) (CDC-like kinase 3) |
2.7.12.1 | Homo sapiens | 6ft7_b | P49761 | ENSG00000179335 | CLK3 | 98.30 | 1.40E-10 | 1.70E-14 | 114.30 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR216C | SKY1 | SGDID:S000004829 | GSK3B |
Glycogen synthase kinase-3 beta (GSK-3 beta) (EC 2.7.11.26) (Serine/threonine-protein kinase GSK3B) (EC 2.7.11.1) |
2.7.11.26 | Homo sapiens | Liver Disease,Endometrial Cancer,Epilepsy,Polycystic Kidney Disease,Diabetes Mellitus,Alzheimer Disease,Major Depressive Disorder,Neuroblastoma,Cervical Non-Keratinizing Squamous Cell Carcinoma,Barbiturate Dependence,Alzheimer Disease 9,Dementia,Fallopian Tube Serous Adenocarcinoma,Breast Cancer,Parkinson Disease, Late-Onset,Colorectal Cancer,Parkinson Disease 1, Autosomal Dominant,Hepatocellular Carcinoma,Bipolar Disorder,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Type 2 Diabetes Mellitus,Schizophrenia,Ophthalmomyiasis,Familial Adenomatous Polyposis,Severe Congenital Neutropenia,Aneurysmal Bone Cysts,Attention Deficit-Hyperactivity Disorder,Medulloblastoma,Frontotemporal Dementia,Pancreatic Cancer |
1h8f_a | P49841 | ENSG00000082701 | GSK3B | 97.90 | 2.80E-09 | 3.10E-13 | 105.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CDK7 CAK CAK1 CDKN7 MO15 STK1 |
Cyclin-dependent kinase 7 (EC 2.7.11.22) (EC 2.7.11.23) (39 kDa protein kinase) (p39 Mo15) (CDK-activating kinase 1) (Cell division protein kinase 7) (Serine/threonine-protein kinase 1) (TFIIH basal transcription factor complex kinase subunit) |
2.7.11.22,2.7.11.23, | Homo sapiens | Myofibrillar Myopathy,Cockayne Syndrome,Breast Cancer,Xeroderma Pigmentosum, Complementation Group D,Xeroderma Pigmentosum, Variant Type,Xeroderma Pigmentosum, Complementation Group B |
1ua2_b | P50613 | ENSG00000134058 | CDK7 | 98.10 | 1.10E-09 | 1.30E-13 | 107.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CDK9 CDC2L4 TAK |
Cyclin-dependent kinase 9 (EC 2.7.11.22) (EC 2.7.11.23) (C-2K) (Cell division cycle 2-like protein kinase 4) (Cell division protein kinase 9) (Serine/threonine-protein kinase PITALRE) (Tat-associated kinase complex catalytic subunit) |
2.7.11.22,2.7.11.23, | Homo sapiens | Leukemia, Acute Myeloid,Human Immunodeficiency Virus Type 1,Immune Deficiency Disease,Leukemia, Chronic Lymphocytic,Nut Midline Carcinoma |
3mi9_a | P50750 | ENSG00000136807 | CDK9 | 97.80 | 1.00E-08 | 1.10E-12 | 101.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | RPS6KA3 ISPK1 MAPKAPK1B RSK2 |
Ribosomal protein S6 kinase alpha-3 (S6K-alpha-3) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 3) (p90-RSK 3) (p90RSK3) (Insulin-stimulated protein kinase 1) (ISPK-1) (MAP kinase-activated protein kinase 1b) (MAPK-activated protein kinase 1b) (MAPKAP kinase 1b) (MAPKAPK-1b) (Ribosomal S6 kinase 2) (RSK-2) (pp90RSK2) |
2.7.11.1 | Homo sapiens | Ventricular Septal Defect,Learning Disability,Symptomatic Form Of Coffin-Lowry Syndrome In Female Carriers,Cohen Syndrome,Specific Learning Disability,Gastroesophageal Reflux,Breast Cancer,Cardiomyopathy, Familial Hypertrophic, 4,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Chromosome 16p13.3 Deletion Syndrome, Proximal,Orthostatic Intolerance,Dyskeratosis Congenita, Autosomal Dominant 3,X-Linked Monogenic Disease,Non-Syndromic X-Linked Intellectual Disability,Coffin-Lowry Syndrome,Hypertelorism,Partington X-Linked Mental Retardation Syndrome,Scoliosis |
4d9u_a | P51812 | ENSG00000177189 | RPS6KA3 | 98.00 | 2.20E-09 | 2.50E-13 | 106.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MAP2K6 MEK6 MKK6 PRKMK6 SKK3 |
Dual specificity mitogen-activated protein kinase kinase 6 (MAP kinase kinase 6) (MAPKK 6) (EC 2.7.12.2) (MAPK/ERK kinase 6) (MEK 6) (Stress-activated protein kinase kinase 3) (SAPK kinase 3) (SAPKK-3) (SAPKK3) |
2.7.12.2 | Homo sapiens | Human Cytomegalovirus Infection,Anthrax Disease,Cardiomyopathy, Familial Hypertrophic, 25 |
3fme_a | P52564 | ENSG00000108984 | MAP2K6 | 97.70 | 1.20E-08 | 1.50E-12 | 95.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | DAPK1 DAPK |
Death-associated protein kinase 1 (DAP kinase 1) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Squamous Cell Carcinoma,Childhood Acute Lymphocytic Leukemia,Lung Cancer Susceptibility 3,Adenoid Cystic Carcinoma,Cholecystitis,Alzheimer Disease,B-Cell Lymphoma,Mixed Oligodendroglioma-Astrocytoma,Transitional Cell Carcinoma,Bladder Cancer,Tuberous Sclerosis 2,Parkinson Disease, Late-Onset,Colorectal Cancer,Pediatric Lymphoma,Oligodendroglioma,Central Neurocytoma,Ischemia,Gastric Cancer,Pancreatic Ductal Adenocarcinoma,Cholangiocarcinoma,Cervical Cancer,Cervical Squamous Cell Carcinoma,Myelodysplastic Syndrome,Nasopharyngeal Carcinoma,Lung Cancer |
2w4k_a | P53355 | ENSG00000196730 | DAPK1 | 97.80 | 9.00E-09 | 1.00E-12 | 98.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | LIMK1 LIMK |
LIM domain kinase 1 (LIMK-1) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Breast Cancer,Intracranial Aneurysm,Prostate Cancer,Disease Of Mental Health,Fragile X Syndrome,Supravalvular Aortic Stenosis,Williams-Beuren Syndrome,Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease |
5hvk_a | P53667 | ENSG00000106683 | LIMK1 | 97.90 | 3.10E-09 | 3.60E-13 | 101.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MAPK10 JNK3 JNK3A PRKM10 SAPK1B |
Mitogen-activated protein kinase 10 (MAP kinase 10) (MAPK 10) (EC 2.7.11.24) (MAP kinase p49 3F12) (Stress-activated protein kinase 1b) (SAPK1b) (Stress-activated protein kinase JNK3) (c-Jun N-terminal kinase 3) |
2.7.11.24 | Homo sapiens | Cryptococcal Meningitis,Diabetes Mellitus,Alzheimer Disease,Amyotrophic Lateral Sclerosis 1,Cataract,Breast Cancer,Parkinson Disease, Late-Onset,Human Immunodeficiency Virus Type 1,Pheochromocytoma,Pertussis,Opioid Abuse,Type 2 Diabetes Mellitus,Lennox-Gastaut Syndrome,Huntington Disease,Pancreatic Cancer |
3oy1_a | P53779 | ENSG00000109339 | MAPK10 | 98.40 | 3.80E-11 | 4.30E-15 | 120.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | PRKAA2 AMPK AMPK2 |
5'-AMP-activated protein kinase catalytic subunit alpha-2 (AMPK subunit alpha-2) (EC 2.7.11.1) (Acetyl-CoA carboxylase kinase) (ACACA kinase) (EC 2.7.11.27) (Hydroxymethylglutaryl-CoA reductase kinase) (HMGCR kinase) (EC 2.7.11.31) |
2.7.11.27,2.7.11.31, | Homo sapiens | Hyperglycemia,Hypertrophic Cardiomyopathy,Glycogen Storage Disease,Phosphorylase Kinase Deficiency,Tuberous Sclerosis,Breast Cancer,Ischemia,Aromatase Deficiency,Peutz-Jeghers Syndrome,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Wolff-Parkinson-White Syndrome |
2h6d_a | P54646 | ENSG00000162409 | PRKAA2 | 97.70 | 1.30E-08 | 1.50E-12 | 95.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CSNK2A1 CK2A1 |
Casein kinase II subunit alpha (CK II alpha) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Okur-Chung Neurodevelopmental Syndrome,Connective Tissue Disease,Alzheimer Disease,Prostate Stromal Sarcoma,Distal Muscular Dystrophy With Anterior Tibial Onset,Kidney Leiomyosarcoma,Colorectal Cancer,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Prostate Cancer,Disease Of Mental Health,Malaria |
3q04_a | P68400 | ENSG00000101266 | CSNK2A1 | 98.00 | 1.60E-09 | 1.90E-13 | 104.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | pknI Rv2914c MTCY338.02c |
Serine/threonine-protein kinase PknI (EC 2.7.11.1) |
2.7.11.1 | Mycobacterium tuberculosis | 5xka_b | P9WI69 | 98.20 | 5.10E-10 | 5.90E-14 | 106.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | CDKL1 |
Cyclin-dependent kinase-like 1 (EC 2.7.11.22) (Protein kinase p42 KKIALRE) (Serine/threonine-protein kinase KKIALRE) |
2.7.11.22 | Homo sapiens | Fraser Syndrome 1 |
4agu_b | Q00532 | ENSG00000100490 | CDKL1 | 97.80 | 9.90E-09 | 1.10E-12 | 98.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CDK5 CDKN5 |
Cyclin-dependent-like kinase 5 (EC 2.7.11.1) (Cell division protein kinase 5) (Serine/threonine-protein kinase PSSALRE) (Tau protein kinase II catalytic subunit) (TPKII catalytic subunit) |
2.7.11.1 | Homo sapiens | Cerebellar Hypoplasia,Supranuclear Palsy, Progressive, 1,Polycystic Kidney Disease,Dyslexia,Alzheimer Disease,Amyotrophic Lateral Sclerosis 1,Transient Cerebral Ischemia,Giant Axonal Neuropathy 2,Motor Neuron Disease,Neuroblastoma,Hereditary Spastic Paraplegia,Nephronophthisis,Alzheimer Disease 9,Scrapie,Parkinson Disease, Late-Onset,Lissencephaly With Cerebellar Hypoplasia,Pick Disease Of Brain,Ischemia,Developmental And Epileptic Encephalopathy 5,Disease Of Mental Health,Toxic Encephalopathy,Dementia, Lewy Body,Lissencephaly,Aneurysmal Bone Cysts,Lissencephaly 7 With Cerebellar Hypoplasia,Syndromic Intellectual Disability,Non-Syndromic Intellectual Disability,Multiple System Atrophy 1,Myasthenic Syndrome, Congenital, 19,Primary Autosomal Recessive Microcephaly,C Syndrome,Lung Cancer |
4au8_b | Q00535 | ENSG00000164885 | CDK5 | 98.30 | 1.70E-10 | 2.00E-14 | 109.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CDK16 PCTAIRE1 PCTK1 |
Cyclin-dependent kinase 16 (EC 2.7.11.22) (Cell division protein kinase 16) (PCTAIRE-motif protein kinase 1) (Serine/threonine-protein kinase PCTAIRE-1) |
2.7.11.22 | Homo sapiens | 5g6v_a | Q00536 | ENSG00000102225 | CDK16 | 97.80 | 6.20E-09 | 6.80E-13 | 102.30 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR216C | SKY1 | SGDID:S000004829 | MAP2K1 MEK1 PRKMK1 |
Dual specificity mitogen-activated protein kinase kinase 1 (MAP kinase kinase 1) (MAPKK 1) (MKK1) (EC 2.7.12.2) (ERK activator kinase 1) (MAPK/ERK kinase 1) (MEK 1) |
2.7.12.2 | Homo sapiens | Melorheostosis, Isolated,Skin Melanoma,Achondroplasia,Heart Disease,Ichthyosis,Squamous Cell Carcinoma,Cerebral Hemisphere Lipoma,Corpus Callosum Lipoma,Lung Cancer Susceptibility 3,Melorheostosis,Pulmonary Valve Stenosis,Suppression Of Tumorigenicity 12,Melanoma,Acneiform Dermatitis,Neurofibromatosis-Noonan Syndrome,Hypertrophic Cardiomyopathy,Osteopoikilosis,Alzheimer Disease,Rasopathy,Noonan Syndrome-Like Disorder With Loose Anagen Hair,Keratosis Pilaris Atrophicans Faciei,Costello Syndrome,Anthrax Disease,Extracranial Arteriovenous Malformation,Neurofibromatosis, Type I,Neuroblastoma,Skin Granular Cell Tumor,Pseudo-Turner Syndrome,Leukemia, Acute Myeloid,Noonan Syndrome 1,Senile Angioma,Hemangioma,Rosai-Dorfman Disease,Bladder Cancer,Mixed Cell Adenoma,Hairy Cell Leukemia,Prostate Squamous Cell Carcinoma,Noonan Syndrome-Like Disorder With Loose Anagen Hair 2,Cardiofaciocutaneous Syndrome 3,Ovarian Cancer,Myeloid Leukemia,Adenocarcinoma,Breast Cancer,Squamous Cell Carcinoma, Head And Neck,Colorectal Cancer,Pulmonary Valve Disease,Hepatocellular Carcinoma,Cardiofaciocutaneous Syndrome 1,Splenic Diffuse Red Pulp Small B-Cell Lymphoma,Pheochromocytoma,Rhabdomyosarcoma,Noonan Syndrome With Multiple Lentigines,Fibrosarcoma,Histiocytosis,Skin Carcinoma,Gastric Cancer,Arteriovenous Malformation,Prostate Cancer,Disease Of Mental Health,Gastric Adenocarcinoma,Langerhans Cell Histiocytosis,Bladder Urothelial Carcinoma,Lymphoma, Non-Hodgkin, Familial,Diamond-Blackfan Anemia 20,Acute Promyelocytic Leukemia,Ovarian Melanoma,Autism Spectrum Disorder,Kaposi Sarcoma,Cardiomyopathy, Familial Hypertrophic, 25,Medulloblastoma,Autism,Melanoma, Cutaneous Malignant 1,Melanoma, Uveal,Lung Cancer,Pancreatic Cancer |
3eqc_a | Q02750 | ENSG00000169032 | MAP2K1 | 97.90 | 3.40E-09 | 3.80E-13 | 105.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | SKY1 YMR216C YM8261.10C |
Serine/threonine-protein kinase SKY1 (SRPK) (EC 2.7.11.1) |
2.7.11.1 | Saccharomyces cerevisiae | 1q8y_b | Q03656 | 100.00 | 8.20E-35 | 9.20E-39 | 297.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | BTK AGMX1 ATK BPK |
Tyrosine-protein kinase BTK (EC 2.7.10.2) (Agammaglobulinemia tyrosine kinase) (ATK) (B-cell progenitor kinase) (BPK) (Bruton tyrosine kinase) |
2.7.10.2 | Homo sapiens | Pneumocystosis,X-Linked Recessive Disease,Lymphopenia,Conjunctivitis,Richter'S Syndrome,Macroglobulinemia,Pyoderma,Cll/Sll,Mast-Cell Leukemia,Polyarticular Juvenile Idiopathic Arthritis,Spherocytosis, Type 5,Ecthyma,B Cell Deficiency,Lung Large Cell Carcinoma,B-Cell Lymphoma,Common Variable Immunodeficiency,Neutropenia,Agammaglobulinemia 1, Autosomal Recessive,Plasma Protein Metabolism Disease,Isolated Agammaglobulinemia,Poliomyelitis,Leukemia, Acute Myeloid,Growth Hormone Deficiency,Leukemia, Acute Lymphoblastic,Agammaglobulinemia,Bacterial Infectious Disease,Breast Cancer,Central Nervous System Hematologic Cancer,Congenital Hypogammaglobulinemia,Immunodeficiency 14,Panniculitis,Immunodeficiency 33,Lymphoma, Non-Hodgkin, Familial,Baylisascariasis,Agammaglobulinemia, X-Linked,Paralytic Poliomyelitis,Immune Deficiency Disease,Myelodysplastic Syndrome,Immunoglobulin A Deficiency 1,Wiskott-Aldrich Syndrome,X-Linked Monogenic Disease,Diffuse Large B-Cell Lymphoma,Mantle Cell Lymphoma,Lymphoplasmacytic Lymphoma,Marginal Zone B-Cell Lymphoma,Splenic Marginal Zone Lymphoma,Williams-Beuren Syndrome,Combined Oxidative Phosphorylation Deficiency 9,Mohr-Tranebjaerg Syndrome,Cd40 Ligand Deficiency,Isolated Growth Hormone Deficiency, Type Iii, With Agammaglobulinemia,Immunodeficiency 45,Immunodeficiency With Hyper-Igm, Type 1,Leukemia, Chronic Lymphocytic,Myeloma, Multiple,Isolated Growth Hormone Deficiency,Isolated Growth Hormone Deficiency Type Iii,Waldenstroem'S Macroglobulinemia |
5p9j_a | Q06187 | ENSG00000010671 | BTK | 98.10 | 8.30E-10 | 9.70E-14 | 103.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | Rop2 |
Rop2 |
Toxoplasma gondii | 3dzo_a | Q06AK3 | 97.80 | 7.40E-09 | 8.00E-13 | 106.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | CRK2 PK5 |
Cell division control protein 2 homolog (EC 2.7.11.22) (EC 2.7.11.23) (PfPK5) |
2.7.11.22,2.7.11.23, | Plasmodium falciparum | 1v0b_a | Q07785 | 98.00 | 2.70E-09 | 3.10E-13 | 101.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | STK4 KRS2 MST1 |
Serine/threonine-protein kinase 4 (EC 2.7.11.1) (Mammalian STE20-like protein kinase 1) (MST-1) (STE20-like kinase MST1) (Serine/threonine-protein kinase Krs-2) [Cleaved into: Serine/threonine-protein kinase 4 37kDa subunit (MST1/N); Serine/threonine-protein kinase 4 18kDa subunit (MST1/C)] |
2.7.11.1 | Homo sapiens | T-Cell Immunodeficiency, Recurrent Infections, And Autoimmunity With Or Without Cardiac Malformations,Myeloproliferative Syndrome, Transient,Lymphoproliferative Syndrome 2,Epidermodysplasia Verruciformis 1,Immunodeficiency 13,Prostate Cancer,Coronin-1a Deficiency,Wilson-Turner X-Linked Mental Retardation Syndrome,Lung Cancer |
3com_a | Q13043 | ENSG00000101109 | STK4 | 97.70 | 1.20E-08 | 1.30E-12 | 98.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MAPK7 BMK1 ERK5 PRKM7 |
Mitogen-activated protein kinase 7 (MAP kinase 7) (MAPK 7) (EC 2.7.11.24) (Big MAP kinase 1) (BMK-1) (Extracellular signal-regulated kinase 5) (ERK-5) |
2.7.11.24 | Homo sapiens | Bone Cancer,Noma,Primary Bone Cancer,Dilated Cardiomyopathy,Breast Cancer,Prostate Cancer,Osteogenesis Imperfecta, Type Xviii,Scoliosis, Isolated 1,Scoliosis |
4zsg_a | Q13164 | ENSG00000166484 | MAPK7 | 98.20 | 4.20E-10 | 4.80E-14 | 110.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | STK3 KRS1 MST2 |
Serine/threonine-protein kinase 3 (EC 2.7.11.1) (Mammalian STE20-like protein kinase 2) (MST-2) (STE20-like kinase MST2) (Serine/threonine-protein kinase Krs-1) [Cleaved into: Serine/threonine-protein kinase 3 36kDa subunit (MST2/N); Serine/threonine-protein kinase 3 20kDa subunit (MST2/C)] |
2.7.11.1 | Homo sapiens | Non-Syndromic X-Linked Intellectual Disability |
4lg4_a | Q13188 | ENSG00000104375 | STK3 | 98.50 | 1.90E-11 | 2.20E-15 | 117.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | PRPF4B KIAA0536 PRP4 PRP4H PRP4K |
Serine/threonine-protein kinase PRP4 homolog (EC 2.7.11.1) (PRP4 kinase) (PRP4 pre-mRNA-processing factor 4 homolog) |
2.7.11.1 | Homo sapiens | 4iir_a | Q13523 | ENSG00000112739 | PRPF4B | 97.90 | 4.40E-09 | 4.90E-13 | 104.50 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR216C | SKY1 | SGDID:S000004829 | CAMK2D CAMKD |
Calcium/calmodulin-dependent protein kinase type II subunit delta (CaM kinase II subunit delta) (CaMK-II subunit delta) (EC 2.7.11.17) |
2.7.11.17 | Homo sapiens | Dilated Cardiomyopathy,Cardiomyopathy, Dilated, 1dd |
2wel_a | Q13557 | ENSG00000145349 | CAMK2D | 97.80 | 8.00E-09 | 9.00E-13 | 100.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | DYRK1A DYRK MNB MNBH |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A (EC 2.7.12.1) (Dual specificity YAK1-related kinase) (HP86) (Protein kinase minibrain homolog) (MNBH) (hMNB) |
2.7.12.1 | Homo sapiens | Chromosomal Disease,Seizure Disorder,Alzheimer Disease,Myeloproliferative Syndrome, Transient,Distal Muscular Dystrophy With Anterior Tibial Onset,Congenital Nervous System Abnormality,Dyrk1a Syndrome,Acute Megakaryocytic Leukemia,Dyrk1a-Related Intellectual Disability Syndrome Due To 21q22.13q22.2 Microdeletion,Microphthalmia,Parkinson Disease, Late-Onset,Non-Specific Syndromic Intellectual Disability,Microcephaly,Intellectual Disability Syndrome Due To A Dyrk1a Point Mutation,Pick Disease Of Brain,Alacrima, Achalasia, And Mental Retardation Syndrome,Enophthalmos,Disease Of Mental Health,Mental Retardation, Autosomal Dominant 7,Down Syndrome,Syndromic Intellectual Disability,Specific Developmental Disorder,Autosomal Dominant Non-Syndromic Intellectual Disability,Chromosomal Duplication Syndrome,Autism,Primary Microcephaly |
4yu2_a | Q13627 | ENSG00000157540 | DYRK1A | 99.20 | 1.40E-15 | 1.60E-19 | 152.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CDK13 CDC2L CDC2L5 CHED KIAA1791 |
Cyclin-dependent kinase 13 (EC 2.7.11.22) (EC 2.7.11.23) (CDC2-related protein kinase 5) (Cell division cycle 2-like protein kinase 5) (Cell division protein kinase 13) (hCDK13) (Cholinesterase-related cell division controller) |
2.7.11.22,2.7.11.23, | Homo sapiens | Corneal Endothelial Dystrophy,Neuroblastoma,Congenital Heart Defects, Dysmorphic Facial Features, And Intellectual Developmental Disorder,Microcephaly,Corneal Dystrophy, Posterior Polymorphous, 1,Spinocerebellar Ataxia 14,Strabismus,White-Sutton Syndrome |
5efq_a | Q14004 | ENSG00000065883 | CDK13 | 98.00 | 2.40E-09 | 2.70E-13 | 105.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MELK KIAA0175 |
Maternal embryonic leucine zipper kinase (hMELK) (EC 2.7.11.1) (Protein kinase Eg3) (pEg3 kinase) (Protein kinase PK38) (hPK38) (Tyrosine-protein kinase MELK) (EC 2.7.10.2) |
2.7.10.2 | Homo sapiens | Colorectal Cancer |
5k00_a | Q14680 | ENSG00000165304 | MELK | 97.80 | 7.70E-09 | 8.50E-13 | 102.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | RPS6KA1 MAPKAPK1A RSK1 |
Ribosomal protein S6 kinase alpha-1 (S6K-alpha-1) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 1) (p90-RSK 1) (p90RSK1) (p90S6K) (MAP kinase-activated protein kinase 1a) (MAPK-activated protein kinase 1a) (MAPKAP kinase 1a) (MAPKAPK-1a) (Ribosomal S6 kinase 1) (RSK-1) |
2.7.11.1 | Homo sapiens | Tuberous Sclerosis 2,Tuberous Sclerosis,Cardiomyopathy, Familial Hypertrophic, 4,Disease Of Mental Health,Adrenal Cortical Adenocarcinoma,Dyskeratosis Congenita, Autosomal Dominant 3,Tuberous Sclerosis 1,Coffin-Lowry Syndrome,Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease |
4nif_d | Q15418 | ENSG00000117676 | RPS6KA1 | 97.90 | 3.20E-09 | 3.50E-13 | 104.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | STK11 LKB1 PJS |
Serine/threonine-protein kinase STK11 (EC 2.7.11.1) (Liver kinase B1) (LKB1) (hLKB1) (Renal carcinoma antigen NY-REN-19) |
2.7.11.1 | Homo sapiens | Skin Melanoma,Squamous Cell Carcinoma,Lung Cancer Susceptibility 3,Cowden Syndrome,Melanoma,Rare Gynecological Tumor,Lung Non-Squamous Non-Small Cell Carcinoma,Cowden Syndrome 1,Cervical Adenoma Malignum,Pulmonary Large Cell Neuroendocrine Carcinoma,B-Lymphoblastic Leukemia/Lymphoma,Large Cell Carcinoma,Pancreatic Intraductal Papillary-Colloid Carcinoma,Inherited Cancer-Predisposing Syndrome,Gynecomastia,Vaginal Tubulovillous Adenoma,Hereditary Mixed Polyposis Syndrome,Hepatocellular Clear Cell Carcinoma,Carney Complex Variant,Intestinal Polyposis Syndrome,Dysplastic Nevus Syndrome,Skin Amelanotic Melanoma,Polyhydramnios,Small Intestine Cancer,Vaginal Adenoma,Testicular Germ Cell Tumor,Long Qt Syndrome,Lip And Oral Cavity Cancer,Ovarian Cancer,Adenocarcinoma,Tuberous Sclerosis 2,Tuberous Sclerosis,Testicular Cancer,Acinar Cell Carcinoma,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Acute Monoblastic Leukemia,Colorectal Cancer,Juvenile Polyposis Syndrome,Peutz-Jeghers Syndrome,Polyposis, Skin Pigmentation, Alopecia, And Fingernail Changes,Skin Carcinoma,Cervical Cancer,Lung Benign Neoplasm,Lynch Syndrome,Lung Squamous Cell Carcinoma,Pancreatic Serous Cystadenoma,Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy,Diamond-Blackfan Anemia 20,Gastric Cancer, Hereditary Diffuse,Tumor Predisposition Syndrome,Tuberous Sclerosis 1,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Intussusception,Vaginal Benign Neoplasm,Li-Fraumeni Syndrome,Ataxia-Telangiectasia,Melanoma, Cutaneous Malignant 1,Lung Cancer,Pancreatic Cancer |
2wtk_c | Q15831 | ENSG00000118046 | STK11 | 97.80 | 5.90E-09 | 6.80E-13 | 99.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | PKN1 PAK1 PKN PRK1 PRKCL1 |
Serine/threonine-protein kinase N1 (EC 2.7.11.13) (Protease-activated kinase 1) (PAK-1) (Protein kinase C-like 1) (Protein kinase C-like PKN) (Protein kinase PKN-alpha) (Protein-kinase C-related kinase 1) (Serine-threonine protein kinase N) |
2.7.11.13 | Homo sapiens | 4otd_a | Q16512 | ENSG00000123143 | PKN1 | 97.80 | 9.90E-09 | 1.10E-12 | 100.50 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR216C | SKY1 | SGDID:S000004829 | MAPK14 CSBP CSBP1 CSBP2 CSPB1 MXI2 SAPK2A |
Mitogen-activated protein kinase 14 (MAP kinase 14) (MAPK 14) (EC 2.7.11.24) (Cytokine suppressive anti-inflammatory drug-binding protein) (CSAID-binding protein) (CSBP) (MAP kinase MXI2) (MAX-interacting protein 2) (Mitogen-activated protein kinase p38 alpha) (MAP kinase p38 alpha) (Stress-activated protein kinase 2a) (SAPK2a) |
2.7.11.24 | Homo sapiens | Psoriasis,Heart Disease,Bladder Lateral Wall Cancer,Leukemia, Chronic Myeloid,Gaucher'S Disease,Alzheimer Disease,Myocardial Infarction,Doxorubicin Induced Cardiomyopathy,Human Cytomegalovirus Infection,Vitreous Abscess,Anthrax Disease,Colon Adenocarcinoma,Autoimmune Disease,Dilated Cardiomyopathy,Ureteral Obstruction,Ovarian Cancer,Tuberous Sclerosis 2,Breast Cancer,Parkinson Disease, Late-Onset,Colorectal Cancer,Hepatocellular Carcinoma,Septic Myocarditis,Pheochromocytoma,Ischemia,Skin Carcinoma,Chlamydia,Prostate Cancer,Disease Of Mental Health,Cholangiocarcinoma,Skin Disease,Retinoblastoma,Rheumatoid Arthritis,Inflammatory Bowel Disease,Trichothiodystrophy 5, Nonphotosensitive,Fibrodysplasia Ossificans Progressiva,Acute Promyelocytic Leukemia,Pulmonary Disease, Chronic Obstructive,Lipoprotein Quantitative Trait Locus,Cardiomyopathy, Familial Hypertrophic, 25,Alexander Disease,Lung Cancer,Osteogenic Sarcoma,Asthma |
2fst_x | Q16539 | ENSG00000112062 | MAPK14 | 98.10 | 7.80E-10 | 8.50E-14 | 111.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CAMK4 CAMK CAMK-GR CAMKIV |
Calcium/calmodulin-dependent protein kinase type IV (CaMK IV) (EC 2.7.11.17) (CaM kinase-GR) |
2.7.11.17 | Homo sapiens | Lung Large Cell Carcinoma,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Crouzon Syndrome With Acanthosis Nigricans,Systemic Lupus Erythematosus,Gingival Fibromatosis |
2w4o_a | Q16566 | ENSG00000152495 | CAMK4 | 97.80 | 8.10E-09 | 8.80E-13 | 103.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | MAPK6 ERK3 PRKM6 |
Mitogen-activated protein kinase 6 (MAP kinase 6) (MAPK 6) (EC 2.7.11.24) (Extracellular signal-regulated kinase 3) (ERK-3) (MAP kinase isoform p97) (p97-MAPK) |
2.7.11.24 | Homo sapiens | Pulmonary Immaturity,Aromatase Excess Syndrome |
2i6l_a | Q16659 | ENSG00000069956 | MAPK6 | 98.00 | 1.40E-09 | 1.70E-13 | 104.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | unc-22 ZK617.1 |
Twitchin (EC 2.7.11.1) (Uncoordinated protein 22) |
2.7.11.1 | Caenorhabditis elegans | 3uto_a | Q23551 | 98.60 | 1.00E-11 | 1.20E-15 | 131.70 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | ROP 2 |
ROP 2 |
Toxoplasma gondii | 2w1z_b | Q27007 | 97.70 | 1.20E-08 | 1.40E-12 | 100.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | AAK1 KIAA1048 |
AP2-associated protein kinase 1 (EC 2.7.11.1) (Adaptor-associated kinase 1) |
2.7.11.1 | Homo sapiens | Parkinson Disease, Late-Onset,Cataract 8, Multiple Types,Hepatitis C Virus,Rabies |
4wsq_a | Q2M2I8 | ENSG00000115977 | AAK1 | 98.30 | 1.50E-10 | 1.70E-14 | 111.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | rop18 ROP18 TGRH88_034260 |
rop18 ROP18 TGRH88_034260 |
Toxoplasma gondii | 4jrn_a | Q2PAY2 | 98.20 | 4.80E-10 | 5.30E-14 | 112.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | MPK6 At2g43790 F18O19.10 |
Mitogen-activated protein kinase 6 (AtMPK6) (MAP kinase 6) (EC 2.7.11.24) |
2.7.11.24 | Arabidopsis thaliana | 6dtl_a | Q39026 | 98.70 | 2.20E-12 | 2.50E-16 | 130.00 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | SRK2I 41K OSKL2 SNRK2.3 At5g66880 MUD21.14 |
Serine/threonine-protein kinase SRK2I (EC 2.7.11.1) (OST1-kinase-like 2) (Protein ATHPROKIN B) (SNF1-related kinase 2.3) (SnRK2.3) |
2.7.11.1 | Arabidopsis thaliana | 3uc3_a | Q39193 | 97.90 | 5.30E-09 | 6.00E-13 | 103.80 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | GSK3 LMJF_18_0270 |
GSK3 LMJF_18_0270 |
2.7.11.1 | Leishmania major | 3e3p_a | Q4QE15 | 98.90 | 1.10E-13 | 1.30E-17 | 138.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | LMJF_10_0200 |
LMJF_10_0200 |
Leishmania major | 3pg1_a | Q4QHJ8 | 97.80 | 1.00E-08 | 1.10E-12 | 101.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | TNNI3K CARK |
Serine/threonine-protein kinase TNNI3K (EC 2.7.11.1) (Cardiac ankyrin repeat kinase) (Cardiac troponin I-interacting kinase) (TNNI3-interacting kinase) |
2.7.11.1 | Homo sapiens | Dilated Cardiomyopathy,Restrictive Cardiomyopathy,Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy,Familial Atrial Fibrillation |
6b5j_b | Q59H18 | ENSG00000259030 | FPGT-TNNI3K | 98.10 | 8.80E-10 | 1.00E-13 | 106.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | cgd5_2510 |
cgd5_2510 |
Cryptosporidium parvum | 3niz_a | Q5CRJ8 | 97.70 | 1.30E-08 | 1.50E-12 | 98.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR216C | SKY1 | SGDID:S000004829 | lpl0262 |
lpl0262 |
2.7.11.1 | Legionella pneumophila | 5ckw_b | Q5WZW9 | 97.80 | 6.90E-09 | 7.40E-13 | 107.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | aurkb-a airk2-a |
Aurora kinase B-A (EC 2.7.11.1) (Aurora/IPL1-related kinase 2-A) (AIRK2-A) (XAIRK2-A) (Serine/threonine-protein kinase 12-A) (Serine/threonine-protein kinase aurora-B-A) (xAurora-B) |
2.7.11.1 | Xenopus laevis | 4c2v_b | Q6DE08 | 97.80 | 5.80E-09 | 6.70E-13 | 98.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | roco4 DDB_G0288251 |
Probable serine/threonine-protein kinase roco4 (EC 2.7.11.1) (Ras of complex proteins and C-terminal of roc 4) |
2.7.11.1 | Dictyostelium discoideum | 4yzn_a | Q6XHB2 | 98.50 | 2.90E-11 | 3.40E-15 | 113.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | STRADA LYK5 STRAD |
STE20-related kinase adapter protein alpha (STRAD alpha) (STE20-related adapter protein) (Serologically defined breast cancer antigen NY-BR-96) |
Homo sapiens | Epilepsy,Polyhydramnios,Endometrial Squamous Cell Carcinoma,Breast Cancer,Megalencephaly,Benign Epilepsy With Centrotemporal Spikes,Scheuermann Disease,Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy |
2wtk_b | Q7RTN6 | ENSG00000266173 | STRADA | 98.70 | 1.80E-12 | 2.00E-16 | 130.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR216C | SKY1 | SGDID:S000004829 | PF3D7_0213400 |
PF3D7_0213400 |
2.7.11.1 | Plasmodium falciparum | 2pmn_x | Q7YTF7 | 98.70 | 2.70E-12 | 3.00E-16 | 128.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | MYLK4 SGK085 |
Myosin light chain kinase family member 4 (EC 2.7.11.1) (Sugen kinase 85) (SgK085) |
2.7.11.1 | Homo sapiens | Cardiomyopathy, Familial Restrictive, 2,Deafness, Autosomal Recessive 17,Deafness, Autosomal Recessive 14,Cardiomyopathy, Familial Restrictive, 3 |
2x4f_a | Q86YV6 | ENSG00000145949 | MYLK4 | 97.90 | 4.10E-09 | 4.50E-13 | 105.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | PF3D7_1445400 |
PF3D7_1445400 |
2.7.11.1 | Plasmodium falciparum | 3llt_a | Q8IL19 | 98.20 | 2.80E-10 | 3.20E-14 | 112.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | MAP4K3 RAB8IPL1 |
Mitogen-activated protein kinase kinase kinase kinase 3 (EC 2.7.11.1) (Germinal center kinase-related protein kinase) (GLK) (MAPK/ERK kinase kinase kinase 3) (MEK kinase kinase 3) (MEKKK 3) |
2.7.11.1 | Homo sapiens | Adult-Onset Still'S Disease |
5j5t_a | Q8IVH8 | ENSG00000011566 | MAP4K3 | 97.90 | 4.70E-09 | 5.20E-13 | 105.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CDKL3 NKIAMRE |
Cyclin-dependent kinase-like 3 (EC 2.7.11.22) (Serine/threonine-protein kinase NKIAMRE) |
2.7.11.22 | Homo sapiens | Orofaciodigital Syndrome Vi |
3zdu_a | Q8IVW4 | ENSG00000006837 | CDKL3 | 97.80 | 1.10E-08 | 1.20E-12 | 99.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | ULK2 KIAA0623 |
Serine/threonine-protein kinase ULK2 (EC 2.7.11.1) (Unc-51-like kinase 2) |
2.7.11.1 | Homo sapiens | 6qau_a | Q8IYT8 | ENSG00000083290 | ULK2 | 97.90 | 2.90E-09 | 3.40E-13 | 99.90 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR216C | SKY1 | SGDID:S000004829 | CAMKK1 CAMKKA |
Calcium/calmodulin-dependent protein kinase kinase 1 (CaM-KK 1) (CaM-kinase kinase 1) (CaMKK 1) (EC 2.7.11.17) (CaM-kinase IV kinase) (Calcium/calmodulin-dependent protein kinase kinase alpha) (CaM-KK alpha) (CaM-kinase kinase alpha) (CaMKK alpha) |
2.7.11.17 | Homo sapiens | Tracheitis |
6ccf_b | Q8N5S9 | ENSG00000004660 | CAMKK1 | 97.80 | 1.10E-08 | 1.30E-12 | 95.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | TTN |
Titin (EC 2.7.11.1) (Connectin) (Rhabdomyosarcoma antigen MU-RMS-40.14) |
2.7.11.1 | Homo sapiens | Muscular Disease,Heart Disease,Constrictive Pericarditis,Congenital Fiber-Type Disproportion,Mitral Valve Insufficiency,Aortic Valve Disease 2,Congenital Structural Myopathy,Myopathy,Amyloidosis,Cardiomyopathy, Dilated, 1e,Syncope,Myofibrillar Myopathy,Atrial Heart Septal Defect,Mitochondrial Dna Depletion Syndrome 12b,Childhood-Onset Progressive Contractures-Limb-Girdle Weakness-Muscle Dystrophy Syndrome,Emery-Dreifuss Muscular Dystrophy,Cortical Thymoma,Muscle Tissue Disease,Morvan'S Fibrillary Chorea,Neuromuscular Disease,Hypertrophic Cardiomyopathy,Familial Isolated Dilated Cardiomyopathy,Rasopathy,Autosomal Dominant Distal Myopathy,Lung Large Cell Carcinoma,Myopathy, Distal, 1,Myositis,Myotonic Dystrophy 1,Systolic Heart Failure,Myopathy, Myofibrillar, 1,Diastolic Heart Failure,Autosomal Recessive Limb-Girdle Muscular Dystrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2a,Muscular Dystrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2g,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2j,Muscular Atrophy,Tibial Muscular Dystrophy,Limb-Girdle Muscular Dystrophy,Arrhythmogenic Right Ventricular Dysplasia, Familial, 1,Epithelial Malignant Thymoma,Hyaline Body Myopathy,Isolated Elevated Serum Creatine Phosphokinase Levels,Noonan Syndrome 1,Newborn Respiratory Distress Syndrome,Thymus Clear Cell Carcinoma,Reducing Body Myopathy,Myocarditis,Atrial Standstill 1,Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 10,Hereditary Proximal Myopathy With Early Respiratory Failure,Dilated Cardiomyopathy,Alcoholic Cardiomyopathy,Lmna-Related Dilated Cardiomyopathy,Thymus Gland Disease,Long Qt Syndrome,Cardiomyopathy, Dilated, 1dd,Heart Conduction Disease,Udd Distal Myopathy - Tibial Muscular Dystrophy,Muscular Dystrophy, Congenital, Lmna-Related,Neuropathy,Perinephritis,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form,Myopathy, Myofibrillar, 3,Sick Sinus Syndrome,Multiminicore Disease,Cardiomyopathy, Familial Hypertrophic, 4,Cardiomyopathy, Dilated, 1a,Congestive Heart Failure,Myopathy, Myofibrillar, 4,Left Ventricular Noncompaction 2,Foot Drop,Myopathy, Myofibrillar, 5,Rhabdomyosarcoma,Rigid Spine Muscular Dystrophy 1,Epidermolysis Bullosa Simplex With Muscular Dystrophy,Thymoma,Thymus Cancer,Dendritic Cell Thymoma,Respiratory Failure,Centronuclear Myopathy,Myopathy, Myofibrillar, 9, With Early Respiratory Failure,Cardiomyopathy, Dilated, 1g,Congenital Myasthenic Syndrome,Cardiomyopathy, Familial Hypertrophic, 9,Cardiomyopathy, Dilated, 1h,Orthostatic Intolerance,Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant,Lung Squamous Cell Carcinoma,Restrictive Cardiomyopathy,Extrinsic Cardiomyopathy,Lambert-Eaton Myasthenic Syndrome,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Muscle Hypertrophy,Salih Myopathy,Nonaka Myopathy,Primary Cutaneous Amyloidosis,Distal Arthrogryposis,Familial Atrial Fibrillation,Hypermethioninemia Due To Adenosine Kinase Deficiency,Atrioventricular Block,Third-Degree Atrioventricular Block,Barth Syndrome,Cardioneuromyopathy With Hyaline Masses And Nemaline Rods,Cardiomyopathy, Familial Hypertrophic, 1,Wolff-Parkinson-White Syndrome,Muscular Dystrophy-Dystroglycanopathy , Type C, 5,Intrinsic Cardiomyopathy,Peripartum Cardiomyopathy,Lipoprotein Quantitative Trait Locus,Atrial Fibrillation,Scoliosis,Muscular Dystrophy, Duchenne Type,Myopathy, Centronuclear, X-Linked,Cardiac Arrest,Inguinal Hernia,Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2,Myasthenia Gravis,Left Ventricular Noncompaction,Lethal Congenital Contracture Syndrome,Myopathy, Centronuclear, 2,Batten-Turner Congenital Myopathy,Miyoshi Muscular Dystrophy,Tibial Muscular Dystrophy, Tardive,Cardiomyopathy, Dilated, 1b |
1tki_b | Q8WZ42 | ENSG00000155657 | TTN | 98.10 | 1.10E-09 | 1.20E-13 | 107.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | DYRK2 |
Dual specificity tyrosine-phosphorylation-regulated kinase 2 (EC 2.7.12.1) |
2.7.12.1 | Homo sapiens | 4azf_a | Q92630 | ENSG00000127334 | DYRK2 | 99.30 | 2.00E-16 | 2.20E-20 | 164.40 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR216C | SKY1 | SGDID:S000004829 | CDKL2 |
Cyclin-dependent kinase-like 2 (EC 2.7.11.22) (Protein kinase p56 KKIAMRE) (Serine/threonine-protein kinase KKIAMRE) |
2.7.11.22 | Homo sapiens | Papillary Serous Adenocarcinoma,Orofaciodigital Syndrome Vi |
4aaa_a | Q92772 | ENSG00000138769 | CDKL2 | 97.90 | 2.80E-09 | 3.10E-13 | 105.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | PBK TOPK |
Lymphokine-activated killer T-cell-originated protein kinase (EC 2.7.12.2) (Cancer/testis antigen 84) (CT84) (MAPKK-like protein kinase) (Nori-3) (PDZ-binding kinase) (Spermatogenesis-related protein kinase) (SPK) (T-LAK cell-originated protein kinase) |
2.7.12.2 | Homo sapiens | Fuchs' Endothelial Dystrophy,Hematologic Cancer,Plexiform Neurofibroma,Cicatricial Entropion,Malignant Peripheral Nerve Sheath Tumor,Corneal Edema |
5j0a_b | Q96KB5 | ENSG00000168078 | PBK | 98.00 | 1.50E-09 | 1.80E-13 | 102.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CAMK1G CLICK3 VWS1 |
Calcium/calmodulin-dependent protein kinase type 1G (EC 2.7.11.17) (CaM kinase I gamma) (CaM kinase IG) (CaM-KI gamma) (CaMKI gamma) (CaMKIG) (CaMK-like CREB kinase III) (CLICK III) |
2.7.11.17 | Homo sapiens | 2jam_a | Q96NX5 | ENSG00000008118 | CAMK1G | 97.80 | 1.00E-08 | 1.20E-12 | 99.40 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR216C | SKY1 | SGDID:S000004829 | PASK KIAA0135 |
PAS domain-containing serine/threonine-protein kinase (PAS-kinase) (PASKIN) (hPASK) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Niemann-Pick Disease, Type C1 |
3dls_a | Q96RG2 | ENSG00000115687 | PASK | 97.90 | 5.70E-09 | 6.30E-13 | 103.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CAMKK2 CAMKKB KIAA0787 |
Calcium/calmodulin-dependent protein kinase kinase 2 (CaM-KK 2) (CaM-kinase kinase 2) (CaMKK 2) (EC 2.7.11.17) (Calcium/calmodulin-dependent protein kinase kinase beta) (CaM-KK beta) (CaM-kinase kinase beta) (CaMKK beta) |
2.7.11.17 | Homo sapiens | Parkinson Disease, Late-Onset |
5uy6_a | Q96RR4 | ENSG00000110931 | CAMKK2 | 97.90 | 3.00E-09 | 3.50E-13 | 100.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | SRPK1 |
SRSF protein kinase 1 (EC 2.7.11.1) (SFRS protein kinase 1) (Serine/arginine-rich protein-specific kinase 1) (SR-protein-specific kinase 1) |
2.7.11.1 | Homo sapiens | Denys-Drash Syndrome,Lung Cancer |
5my8_a | Q96SB4 | ENSG00000096063 | SRPK1 | 99.70 | 9.50E-22 | 1.10E-25 | 201.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | PKMYT1 MYT1 |
Membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase (EC 2.7.11.1) (Myt1 kinase) |
2.7.11.1 | Homo sapiens | 5vcy_a | Q99640 | ENSG00000127564 | PKMYT1 | 99.00 | 8.00E-14 | 9.10E-18 | 135.60 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR216C | SKY1 | SGDID:S000004829 | MAP3K5 ASK1 MAPKKK5 MEKK5 |
Mitogen-activated protein kinase kinase kinase 5 (EC 2.7.11.25) (Apoptosis signal-regulating kinase 1) (ASK-1) (MAPK/ERK kinase kinase 5) (MEK kinase 5) (MEKK 5) |
2.7.11.25 | Homo sapiens | Liver Disease,Non-Alcoholic Fatty Liver Disease,Pyriform Sinus Cancer,Fatty Liver Disease,Alzheimer Disease,Glottis Squamous Cell Carcinoma,Partial Third-Nerve Palsy,Neural Tube Defects,Huntington Disease |
5uox_a | Q99683 | ENSG00000197442 | MAP3K5 | 97.80 | 9.40E-09 | 1.10E-12 | 95.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | WNK3 KIAA1566 PRKWNK3 |
Serine/threonine-protein kinase WNK3 (EC 2.7.11.1) (Protein kinase lysine-deficient 3) (Protein kinase with no lysine 3) |
2.7.11.1 | Homo sapiens | Bartter Disease,Renal Tubular Transport Disease,Pseudohypoaldosteronism,Agenesis Of The Corpus Callosum With Peripheral Neuropathy,Arthrogryposis, Distal, Type 3,Liddle Syndrome 1,Hypomagnesemia 4, Renal,Distal Arthrogryposis,Hypertension, Essential,Syndromic X-Linked Intellectual Disability Siderius Type,Gitelman Syndrome |
5o2c_a | Q9BYP7 | ENSG00000196632 | WNK3 | 98.00 | 1.80E-09 | 1.90E-13 | 109.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | BSK8 At5g41260 K1O13.5 |
Serine/threonine-protein kinase BSK8 (EC 2.7.11.1) (Brassinosteroid-signaling kinase 8) |
2.7.11.1 | Arabidopsis thaliana | 4i93_b | Q9FHD7 | 98.40 | 5.50E-11 | 6.30E-15 | 114.40 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
| YMR216C | SKY1 | SGDID:S000004829 | PEAK1 KIAA2002 |
Inactive tyrosine-protein kinase PEAK1 (Pseudopodium-enriched atypical kinase 1) (Sugen kinase 269) (Tyrosine-protein kinase SgK269) |
Homo sapiens | 6bhc_a | Q9H792 | ENSG00000173517 | PEAK1 | 98.10 | 8.40E-10 | 9.00E-14 | 114.60 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YMR216C | SKY1 | SGDID:S000004829 | SNRK KIAA0096 SNFRK |
SNF-related serine/threonine-protein kinase (EC 2.7.11.1) (SNF1-related kinase) |
2.7.11.1 | Homo sapiens | Breast Angiosarcoma,Skin Angiosarcoma,Liver Angiosarcoma,Skin Sarcoma,Lymphangiosarcoma,Breast Sarcoma,Hydrolethalus Syndrome 1,Neuronopathy, Distal Hereditary Motor, Type Viii |
5yks_b | Q9NRH2 | ENSG00000163788 | SNRK | 98.60 | 5.30E-12 | 5.60E-16 | 128.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | CDK12 CRK7 CRKRS KIAA0904 |
Cyclin-dependent kinase 12 (EC 2.7.11.22) (EC 2.7.11.23) (Cdc2-related kinase, arginine/serine-rich) (CrkRS) (Cell division cycle 2-related protein kinase 7) (CDC2-related protein kinase 7) (Cell division protein kinase 12) (hCDK12) |
2.7.11.22,2.7.11.23, | Homo sapiens | Lung Cancer Susceptibility 3,Bartholin'S Gland Adenocarcinoma,Corneal Endothelial Dystrophy,Gastric Cancer,Lung Cancer |
4cxa_c | Q9NYV4 | ENSG00000167258 | CDK12 | 97.80 | 1.00E-08 | 1.20E-12 | 100.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YMR216C | SKY1 | SGDID:S000004829 | EIF2AK3 PEK PERK |
Eukaryotic translation initiation factor 2-alpha kinase 3 (EC 2.7.11.1) (PRKR-like endoplasmic reticulum kinase) (Pancreatic eIF2-alpha kinase) (HsPEK) |
2.7.11.1 | Homo sapiens | Skin Melanoma,Retinitis Pigmentosa,Neonatal Diabetes,Prion Disease,Diabetes Mellitus,Alzheimer Disease,Rasopathy,Retinal Degeneration,Subungual Glomus Tumor,Crisponi/Cold-Induced Sweating Syndrome 1,Osteoporosis,Wolfram Syndrome,Epiphyseal Dysplasia, Multiple, With Early-Onset Diabetes Mellitus,Disease Of Mental Health,Leukoencephalopathy With Vanishing White Matter,Odontochondrodysplasia,Trichothiodystrophy 5, Nonphotosensitive,Cardiomyopathy, Familial Hypertrophic, 25,Permanent Neonatal Diabetes Mellitus,Palmoplantar Keratoderma, Bothnian Type |
4x7k_a | Q9NZJ5 | ENSG00000172071 | EIF2AK3 | 97.90 | 5.50E-09 | 6.40E-13 | 99.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |