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AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

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YGR188C BUB1 / SGDID:S000003420
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
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
YGR188C BUB1 SGDID:S000003420
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 99.80 5.30E-24 5.80E-28 217.80 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
BubR1 13 31 BcDNA:LD23835 BUB1 Bub1 bub1 BUBR1 bubR1 bubr1 CG 7838 dBUB1 DmBUB1 Dmbub1 DmBubRI Dmel\CG7838 l(2)k03113 l(2)k06109 mcl(2)Z1525 CG7838 Dmel_CG7838
BubR1 13 31 BcDNA:LD23835 BUB1 Bub1 bub1 BUBR1 bubR1 bubr1 CG 7838 dBUB1 DmBUB1 Dmbub1 DmBubRI Dmel\CG7838 l(2)k03113 l(2)k06109 mcl(2)Z1525 CG7838 Dmel_CG7838
Drosophila melanogaster
6jkk_a A1Z6I7 99.30 1.20E-16 1.60E-20 153.80 0 0 0 0 1 0 0 0
YGR188C BUB1 SGDID:S000003420
BUB1 SCY_2082
BUB1 SCY_2082
Saccharomyces cerevisiae
3esl_b A6ZUJ9 99.90 5.10E-27 5.50E-31 228.30 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
BN1205_040370 TGVEG_207820
BN1205_040370 TGVEG_207820
2.7.11.24 Toxoplasma gondii
3rp9_a B6KP12 99.10 3.50E-15 4.50E-19 151.70 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
Prag1 Pragmin
Inactive tyrosine-protein kinase PRAG1 (PEAK1-related kinase-activating pseudokinase 1) (Pragma of Rnd2)
Rattus norvegicus
6ewx_a D3ZMK9 99.10 5.40E-15 6.40E-19 155.50 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
PTSG_10090
PTSG_10090
2.7.11.17 Salpingoeca rosetta
5ig1_b F2UPG5 99.10 3.40E-15 4.30E-19 147.00 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
ROP5C
ROP5C
Toxoplasma gondii
4lv8_a I6ZQR7 99.10 6.60E-15 8.60E-19 144.30 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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
3cok_b O00444 ENSG00000142731 PLK4 99.20 2.70E-15 3.60E-19 140.10 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 3.70E-15 4.60E-19 147.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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
5os3_a O14965 ENSG00000087586 AURKA 99.10 4.10E-15 5.70E-19 136.00 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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
5jzn_a O15075 ENSG00000133083 DCLK1 99.10 4.50E-15 6.10E-19 137.30 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.20 2.20E-15 2.90E-19 141.90 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
ROP8
ROP8
Toxoplasma gondii
3byv_a O15693 99.10 4.00E-15 5.10E-19 147.90 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
BRI1 At4g39400 F23K16.30
Protein BRASSINOSTEROID INSENSITIVE 1 (AtBRI1) (EC 2.7.10.1) (EC 2.7.11.1) (Brassinosteroid LRR receptor kinase)
2.7.10.1,2.7.11.1, Arabidopsis thaliana
5lpy_a O22476 99.20 1.50E-15 2.00E-19 142.70 0 0 0 0 0 0 1 0
YGR188C BUB1 SGDID:S000003420
BUB1 BUB1L
Mitotic checkpoint serine/threonine-protein kinase BUB1 (hBUB1) (EC 2.7.11.1) (BUB1A)
2.7.11.1 Homo sapiens
Cornelia De Lange Syndrome,Polyposis Syndrome, Hereditary Mixed, 1,Polyploidy,Mosaic Variegated Aneuploidy Syndrome,Hereditary Mixed Polyposis Syndrome,Prostate Carcinoma In Situ,Colorectal Cancer,Lynch Syndrome,Polycystic Liver Disease,Cholestasis, Intrahepatic, Of Pregnancy, 1,Primary Autosomal Recessive Microcephaly,Mosaic Variegated Aneuploidy Syndrome 1,Pancreatic Cancer
6f7b_a O43683 ENSG00000169679 BUB1 99.50 2.30E-19 3.10E-23 174.90 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.20 5.30E-16 6.70E-20 155.30 0 0 0 0 0 0 1 0
YGR188C BUB1 SGDID:S000003420
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 99.30 2.80E-16 3.60E-20 159.30 0 0 0 0 0 0 1 0
YGR188C BUB1 SGDID:S000003420
BUB1B BUBR1 MAD3L SSK1
Mitotic checkpoint serine/threonine-protein kinase BUB1 beta (EC 2.7.11.1) (MAD3/BUB1-related protein kinase) (hBUBR1) (Mitotic checkpoint kinase MAD3L) (Protein SSK1)
2.7.11.1 Homo sapiens
Alternating Exotropia,Patau Syndrome,Polyposis Syndrome, Hereditary Mixed, 1,Mosaic Variegated Aneuploidy Syndrome,Hereditary Mixed Polyposis Syndrome,Plexiform Neurofibroma,Breast Cancer,Colorectal Cancer,Microcephaly,Rhabdomyosarcoma,Premature Chromatid Separation Trait,Lynch Syndrome,Mosaic Variegated Aneuploidy Syndrome 2,Primary Autosomal Recessive Microcephaly,Mosaic Variegated Aneuploidy Syndrome 1
5lcw_s O60566 ENSG00000156970 BUB1B 99.10 4.10E-15 4.00E-19 156.50 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
JAK2
Tyrosine-protein kinase JAK2 (EC 2.7.10.2) (Janus kinase 2) (JAK-2)
2.7.10.2 Homo sapiens
Myeloid And Lymphoid Neoplasms Associated With Pdgfra Rearrangement,Chronic Neutrophilic Leukemia,Chronic Myelomonocytic Leukemia,Portal Vein Thrombosis,Polycystic Kidney Disease,Chronic Eosinophilic Leukemia,Leukemia, Chronic Myeloid,Gaucher'S Disease,B-Lymphoblastic Leukemia/Lymphoma, Bcr-Abl1-Like,B-Cell Lymphoma,Acute Erythroid Leukemia,Core Binding Factor Acute Myeloid Leukemia,Hemorrhagic Disease,Blood Platelet Disease,Essential Thrombocythemia,Myeloproliferative Neoplasm,Thrombocytosis,Leptin Deficiency Or Dysfunction,Sm-Ahnmd,Leukemia,Myelophthisic Anemia,Blood Coagulation Disease,Hypereosinophilic Syndrome,Wernicke Encephalopathy,Acquired Von Willebrand Syndrome,Neutrophilia, Hereditary,Acute Leukemia,Central Retinal Vein Occlusion,Thrombophilia,Leukemia, Acute Myeloid,Primary Mediastinal Large B-Cell Lymphoma,Refractory Anemia,Bone Marrow Cancer,Myelodysplastic/Myeloproliferative Neoplasm,Hematologic Cancer,Splenic Infarction,Leukemia, Acute Lymphoblastic,Cebpa-Associated Familial Acute Myeloid Leukemia,Polycythemia,Dilated Cardiomyopathy,Etv6 Thrombocytopenia And Predisposition To Leukemia,Behcet Syndrome,Hepatic Vascular Disease,Antithrombin Iii Deficiency,Splenomegaly,Acquired Polycythemia,Chronic Leukemia,Diamond-Blackfan Anemia,Mixed Lacrimal Gland Cancer,Erythrocytosis, Familial, 8,Vein Disease,Ovarian Cancer,Myeloid Leukemia,Acute Megakaryocytic Leukemia,Crohn'S Disease,Breast Cancer,Colorectal Cancer,Portal Hypertension,Primary Polycythemia,Premature Menopause,Combined Oxidative Phosphorylation Deficiency 16,Benign Essential Hypertension,Deficiency Anemia,Sarcoma,Fibrosarcoma,Systemic Mastocytosis,Prostate Cancer,Disease Of Mental Health,Mastocytosis,Sagittal Sinus Thrombosis,Body Mass Index Quantitative Trait Locus 11,Thrombocytopenia,Renovascular Hypertension,Amegakaryocytic Thrombocytopenia, Congenital,Beta-Thalassemia,Lymphoma, Non-Hodgkin, Familial,Mouth Disease,Lymphoma, Hodgkin, Classic,Erythrocytosis, Familial, 1,Inflammatory Bowel Disease,Severe Congenital Neutropenia,Myelodysplastic Syndrome,Mental Retardation, Autosomal Dominant 33,Down Syndrome,Gastrointestinal Stromal Tumor,Lymphoblastic Leukemia, Acute, With Lymphomatous Features,Thrombocythemia 3,Hypertension, Essential,Ischemic Colitis,Leukemia, Chronic Lymphocytic,Juvenile Myelomonocytic Leukemia,Systemic Lupus Erythematosus,Premature Ovarian Failure 1,Myelofibrosis,Myeloma, Multiple,Medulloblastoma,Atypical Chronic Myeloid Leukemia,Thrombosis,Lung Cancer,Asthma,Budd-Chiari Syndrome,Polycythemia Vera
3krr_a O60674 ENSG00000096968 JAK2 99.10 4.50E-15 6.20E-19 138.30 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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
3kk8_a O62305 99.10 4.90E-15 6.70E-19 137.80 0 0 0 0 0 1 0 0
YGR188C BUB1 SGDID:S000003420
ROCK2 KIAA0619
Rho-associated protein kinase 2 (EC 2.7.11.1) (Rho kinase 2) (Rho-associated, coiled-coil-containing protein kinase 2) (Rho-associated, coiled-coil-containing protein kinase II) (ROCK-II) (p164 ROCK-2)
2.7.11.1 Homo sapiens
Coronary Artery Vasospasm,Dextrocardia,Ureteral Obstruction,Breast Cancer,Tongue Squamous Cell Carcinoma,Hypertension, Essential
4wot_b O75116 ENSG00000134318 ROCK2 99.20 1.50E-15 1.90E-19 153.30 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 5.00E-15 6.90E-19 138.10 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.20 1.20E-15 1.50E-19 151.70 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 3.50E-15 4.80E-19 139.00 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
Abl1 Abl
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 Mus musculus
3kfa_b P00520 99.10 5.20E-15 7.10E-19 137.90 0 0 1 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
SRC
Proto-oncogene tyrosine-protein kinase Src (EC 2.7.10.2) (Proto-oncogene c-Src) (pp60c-src) (p60-Src)
2.7.10.2 Gallus gallus
3u4w_a P00523 99.20 1.40E-15 1.90E-19 140.50 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 3.20E-15 4.40E-19 139.00 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
NTRK1 MTC TRK TRKA
High affinity nerve growth factor receptor (EC 2.7.10.1) (Neurotrophic tyrosine kinase receptor type 1) (TRK1-transforming tyrosine kinase protein) (Tropomyosin-related kinase A) (Tyrosine kinase receptor) (Tyrosine kinase receptor A) (Trk-A) (gp140trk) (p140-TrkA)
2.7.10.1 Homo sapiens
Spitzoid Melanoma,Megacolon,Skin Melanoma,Ganglioneuroblastoma,Follicular Adenoma,Autonomic Neuropathy,Retinitis Pigmentosa,Thyroid Gland Cancer,Adenoid Cystic Carcinoma,Peripheral Nervous System Benign Neoplasm,Autonomic Nervous System Benign Neoplasm,Leukemia, Chronic Myeloid,Thyroid Gland Anaplastic Carcinoma,Peripheral Nervous System Neoplasm,Alzheimer Disease,Chagas Disease,Tall Cell Variant Papillary Carcinoma,Amyotrophic Lateral Sclerosis 1,Diabetic Neuropathy,Differentiated Thyroid Carcinoma,Capillary Lymphangioma,Congenital Mesoblastic Nephroma,Neuropathy, Hereditary Sensory And Autonomic, Type V,Ganglioneuroma,Neuroblastoma,Multiple Endocrine Neoplasia, Type Iib,Neuroaxonal Dystrophy,Hypertrophic Pyloric Stenosis,Pyloric Stenosis,Leukemia, Acute Myeloid,Sensory Peripheral Neuropathy,Ocular Cicatricial Pemphigoid,Congenital Fibrosarcoma,Autonomic Nervous System Neoplasm,Multiple Mucosal Neuroma,Uterine Corpus Sarcoma,Benign Struma Ovarii,Malignant Giant Cell Tumor Of The Tendon Sheath,Thyroid Carcinoma,Small Intestinal Sarcoma,Uterus Leiomyosarcoma,Ntrk1 Congenital Insensitivity To Pain With Anhidrosis,Femoral Cancer,Ovarian Cancer,Neuropathy,Neuropathy, Hereditary Sensory And Autonomic, Type Iii,Charcot-Marie-Tooth Disease,Cortical Senile Cataract,Breast Cancer,Adrenal Neuroblastoma,Colorectal Cancer,Peripheral Nervous System Disease,Squamous Blepharitis,Sweat Gland Disease,Papillary Carcinoma,Premature Menopause,Oligodendroglioma,Angiokeratoma Circumscriptum,Pheochromocytoma,Multiple Endocrine Neoplasia, Type Iia,Tooth Disease,Neurogenic Arthropathy,Anhidrosis,Mesenchymal Cell Neoplasm,Cone-Rod Dystrophy 2,Prostate Cancer,Disease Of Mental Health,Mastocytosis,Pediatric Fibrosarcoma,Olfactory Neuroblastoma,Thyroid Gland Follicular Carcinoma,Thyroid Gland Medullary Carcinoma,Hereditary Sensory Neuropathy,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 2,Trigeminal Neuralgia,Hirschsprung Disease 1,Attention Deficit-Hyperactivity Disorder,Neuropathy, Hereditary Sensory And Autonomic, Type Viii,Neuropathy, Hereditary Sensory And Autonomic, Type Iia,Glucocorticoid Deficiency 1,Thyroid Carcinoma, Familial Medullary,Medulloblastoma,Insensitivity To Pain, Congenital, With Anhidrosis,Pancreatic Cancer
5wr7_a P04629 ENSG00000198400 NTRK1 99.10 6.00E-15 8.10E-19 138.10 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
PRKCB PKCB PRKCB1
Protein kinase C beta type (PKC-B) (PKC-beta) (EC 2.7.11.13)
2.7.11.13 Homo sapiens
Severe Nonproliferative Diabetic Retinopathy,Hyperglycemia,Macroglobulinemia,Diabetic Macular Edema,Microvascular Complications Of Diabetes 5,Diabetes Mellitus,Macular Retinal Edema,B-Cell Lymphoma,Myotonic Dystrophy 1,Primary Biliary Cholangitis,Diabetic Neuropathy,Kidney Disease,Eye Disease,Glioblastoma,Hepatocellular Carcinoma,Type 2 Diabetes Mellitus,Leukemia, Chronic Lymphocytic,Autism,Lung Cancer
2i0e_a P05771 ENSG00000166501 PRKCB 99.10 4.20E-15 5.50E-19 145.20 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
FES FPS
Tyrosine-protein kinase Fes/Fps (EC 2.7.10.2) (Feline sarcoma/Fujinami avian sarcoma oncogene homolog) (Proto-oncogene c-Fes) (Proto-oncogene c-Fps) (p93c-fes)
2.7.10.2 Homo sapiens
Melanoma,Leukemia, Chronic Myeloid,Latent Syphilis,Sjogren-Larsson Syndrome,Leukemia,Myeloid Leukemia,Sarcoma,Ewing Sarcoma Of Bone,Neurofibrosarcoma,Acute Promyelocytic Leukemia,Miller-Dieker Lissencephaly Syndrome,Myopathy, Centronuclear, 2
3cbl_a P07332 ENSG00000182511 FES 99.30 2.20E-16 3.00E-20 153.90 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
RET CDHF12 CDHR16 PTC RET51
Proto-oncogene tyrosine-protein kinase receptor Ret (EC 2.7.10.1) (Cadherin family member 12) (Proto-oncogene c-Ret) [Cleaved into: Soluble RET kinase fragment; Extracellular cell-membrane anchored RET cadherin 120 kDa fragment]
2.7.10.1 Homo sapiens
Spitzoid Melanoma,Megacolon,Neuroendocrine Tumor,Endocrine Gland Cancer,Endometrial Cancer,Intestinal Pseudo-Obstruction,Follicular Adenoma,Retinitis Pigmentosa,Thyroid Gland Cancer,Islet Cell Tumor,Amyloidosis,Renal Hypoplasia,Cakut,Achalasia,Medullary Sponge Kidney,Cowden Syndrome,Solid Adenocarcinoma With Mucin Production,Peripheral Nervous System Benign Neoplasm,Autonomic Nervous System Benign Neoplasm,Waardenburg'S Syndrome,Rare Tumor,Lung Non-Squamous Non-Small Cell Carcinoma,Thyroid Gland Anaplastic Carcinoma,Adenoma,Parathyroid Carcinoma,Sporadic Pheochromocytoma/Secreting Paraganglioma,Primary Peritoneal Carcinoma,Neuronal Intestinal Dysplasia, Type B,B-Lymphoblastic Leukemia/Lymphoma,Neuroma,B-Lymphoblastic Leukemia/Lymphoma With Hypodiploidy,Constipation,Esophagus Leiomyoma,Multicentric Papillary Thyroid Carcinoma,Tall Cell Variant Papillary Carcinoma,Goiter,Thyroiditis,Differentiated Thyroid Carcinoma,Motor Neuron Disease,Neurofibromatosis, Type I,Parathyroid Adenoma,Ganglioneuroma,Lymph Node Disease,Neuroblastoma,Multiple Endocrine Neoplasia, Type Iib,Pilocytic Astrocytoma,Inherited Cancer-Predisposing Syndrome,Hypertrophic Pyloric Stenosis,Testicular Spermatocytic Seminoma,Pyloric Stenosis,Hemangioma,Thyroid Gland Disease,Central Nervous System Hemangioma,Atypical Follicular Adenoma,Carney Complex Variant,Intestinal Obstruction,Struma Ovarii,Multiple Mucosal Neuroma,Pheochromocytoma-Paraganglioma,Hypoganglionosis,Sudden Infant Death Syndrome,Sensorineural Hearing Loss,Malignant Struma Ovarii,Benign Struma Ovarii,Thyroid Carcinoma,Hereditary Paraganglioma-Pheochromocytoma Syndromes,Thyroid Tumor,Hypermobile Ehlers-Danlos Syndrome,Lung Disease,Gingival Hypertrophy,Nodular Goiter,Skin Lipoma,Lichen Amyloidosis,Ovarian Germ Cell Teratoma,Primary Hyperoxaluria,Kidney Disease,Adenocarcinoma,Neurofibromatosis,Hyperparathyroidism,Charcot-Marie-Tooth Disease,Breast Cancer,Renal Agenesis, Bilateral,Adrenal Medulla Cancer,Colorectal Cancer,Gingival Overgrowth,Papillary Carcinoma,Multiple Endocrine Neoplasia,Nonencapsulated Sclerosing Carcinoma,Microcephaly,Pheochromocytoma,Goldberg-Shprintzen Syndrome,Multiple Endocrine Neoplasia, Type Iia,Tooth Disease,Waardenburg Syndrome, Type 4a,Renal Hypodysplasia/Aplasia 3,Hypoparathyroidism,Parathyroid Gland Disease,Primary Hyperparathyroidism,Hypothyroidism,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Multiple Endocrine Neoplasia, Type Iv,Lung Squamous Cell Carcinoma,Thyroid Gland Follicular Carcinoma,Thyroid Gland Medullary Carcinoma,Multiple Endocrine Neoplasia, Type I,Tetralogy Of Fallot,Alveolar Soft Part Sarcoma,Tumor Predisposition Syndrome,Autosomal Genetic Disease,Ewing Sarcoma,Paraganglioma,Hashimoto Thyroiditis,Renal Hypodysplasia/Aplasia 1,Hirschsprung Disease 1,Paraganglioma And Gastric Stromal Sarcoma,Vesicoureteral Reflux 1,Von Hippel-Lindau Syndrome,Parkinson Disease 8, Autosomal Dominant,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Renal Cell Carcinoma, Nonpapillary,Extra-Adrenal Pheochromocytoma,Hypertelorism,Autoimmune Disease Of Endocrine System,Meningioma, Familial,Endocrine Organ Benign Neoplasm,Cardiovascular Organ Benign Neoplasm,Persistent Generalized Lymphadenopathy,Thyroid Carcinoma, Familial Medullary,Medulloblastoma,Central Hypoventilation Syndrome, Congenital,Familial Hypocalciuric Hypercalcemia,Lung Cancer,Pancreatic Cancer
6fek_a P07949 ENSG00000165731 RET 99.10 3.60E-15 4.90E-19 140.20 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
IGF1R
Insulin-like growth factor 1 receptor (EC 2.7.10.1) (Insulin-like growth factor I receptor) (IGF-I receptor) (CD antigen CD221) [Cleaved into: Insulin-like growth factor 1 receptor alpha chain; Insulin-like growth factor 1 receptor beta chain]
2.7.10.1 Homo sapiens
Pancreatic Adenocarcinoma,Bone Disease,Skin Melanoma,Acanthosis Nigricans,Neuroendocrine Tumor,Endometrial Cancer,Autosomal Dominant Polycystic Kidney Disease,Squamous Cell Carcinoma,Hyperglycemia,Lung Cancer Susceptibility 3,Chromosome 15q26-Qter Deletion Syndrome,Rhabdomyosarcoma 2,Polycystic Kidney Disease,Vagina Sarcoma,Melanoma,Thyroid Gland Anaplastic Carcinoma,Diabetes Mellitus,Dedifferentiated Liposarcoma,Hyperinsulinism,Clear Cell Renal Cell Carcinoma,Odontogenic Myxoma,Atypical Teratoid Rhabdoid Tumor,Amelogenesis Imperfecta,Short Syndrome,Graves' Disease,Insulin-Like Growth Factor I,Craniosynostosis,Neuroblastoma,Ring Chromosome 15,Vaginal Endometrial Stromal Sarcoma,Hyperinsulinemic Hypoglycemia,Ring Chromosome,Osteoporosis,Nk-Cell Enteropathy,Ovarian Cancer,Adenocarcinoma,Breast Cancer,Glioblastoma,Colorectal Cancer,Hepatocellular Carcinoma,Malignant Peripheral Nerve Sheath Tumor,Rhabdomyosarcoma,Prostate Embryonal Rhabdomyosarcoma,Myxoid Liposarcoma,Ovarian Disease,Localized Osteosarcoma,Liposarcoma,Skin Carcinoma,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Rhabdoid Cancer,Adrenal Cortical Carcinoma,Type 2 Diabetes Mellitus,Silver-Russell Syndrome 1,Lung Squamous Cell Carcinoma,Adrenal Cortex Disease,Skeletal Muscle Cancer,Muscle Cancer,Beckwith-Wiedemann Syndrome,Sarcoma, Synovial,Esophageal Cancer,Askin'S Tumor,Hypotrichosis 10,Ewing Sarcoma,Lymphangioleiomyomatosis,Donohue Syndrome,Paraganglioma And Gastric Stromal Sarcoma,Renal Cell Carcinoma, Nonpapillary,Wilms Tumor 1,Nijmegen Breakage Syndrome,Amelogenesis Imperfecta, Type Ig,Medulloblastoma,Melanoma, Uveal,Lung Cancer,Osteogenic Sarcoma,Pancreatic Cancer,Polycythemia Vera
5hzn_d P08069 ENSG00000140443 IGF1R 99.10 5.70E-15 7.80E-19 138.20 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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
4knb_a P08581 ENSG00000105976 MET 99.10 4.70E-15 6.40E-19 137.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
HCK
Tyrosine-protein kinase HCK (EC 2.7.10.2) (Hematopoietic cell kinase) (Hemopoietic cell kinase) (p59-HCK/p60-HCK) (p59Hck) (p61Hck)
2.7.10.2 Homo sapiens
Leukemia, Chronic Myeloid,Tinea Favosa,Renal Pelvis Adenocarcinoma,Leukemia, Acute Lymphoblastic,Human Immunodeficiency Virus Type 1,Co-Trimoxazole Allergy,Immune Deficiency Disease
2hck_b P08631 ENSG00000101336 HCK 99.20 5.80E-16 7.60E-20 154.80 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
SRC SRC1
Proto-oncogene tyrosine-protein kinase Src (EC 2.7.10.2) (Proto-oncogene c-Src) (pp60c-src) (p60-Src)
2.7.10.2 Homo sapiens
Pancreatic Adenocarcinoma,Bone Disease,Skin Melanoma,Differentiating Neuroblastoma,Cryptococcal Meningitis,Retinitis Pigmentosa,Myeloid And Lymphoid Neoplasms Associated With Fgfr1 Abnormalities,Lung Cancer Susceptibility 3,Myopathy,Polycystic Kidney Disease,Leukemia, Chronic Myeloid,Gastroesophageal Adenocarcinoma,Bone Sarcoma,Hepatitis B,Rasopathy,Avian Influenza,Myocardial Infarction,Teeth Hard Tissue Disease,Amelogenesis Imperfecta,Essential Thrombocythemia,Neuroblastoma,Leukemia, Acute Myeloid,Cystic Fibrosis,Bone Marrow Cancer,Leukemia, Acute Lymphoblastic,Agammaglobulinemia,Autonomic Nervous System Neoplasm,Bladder Cancer,Osteoporosis,Ovarian Cancer,Pylorus Cancer,Osteopetrosis,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Diamond-Blackfan Anemia 10,Anaplastic Astrocytoma,Colorectal Cancer,Peripheral Nervous System Disease,Hepatocellular Carcinoma,Human Immunodeficiency Virus Type 1,Noonan Syndrome With Multiple Lentigines,Alzheimer Disease 11,Cherubism,Sarcoma,Skin Carcinoma,Cone-Rod Dystrophy 2,Alzheimer Disease 18,Tetanus,Prostate Cancer,Disease Of Mental Health,Signet Ring Cell Adenocarcinoma,Body Mass Index Quantitative Trait Locus 11,Thrombocytopenia,Lynch Syndrome,Lung Squamous Cell Carcinoma,Agammaglobulinemia, X-Linked,Hypotrichosis 1,Wiskott-Aldrich Syndrome,Maturity-Onset Diabetes Of The Young,Acute Promyelocytic Leukemia,Pulmonary Disease, Chronic Obstructive,Hypertension, Essential,Meningioma, Familial,Frank-Ter Haar Syndrome,Estrogen-Receptor Positive Breast Cancer,Estrogen-Receptor Negative Breast Cancer,Coenzyme Q10 Deficiency, Primary, 1,Amelogenesis Imperfecta, Type Ig,Thrombocytopenia 6,Myelofibrosis,Myeloma, Multiple,Medulloblastoma,Lung Cancer,Pancreatic Cancer,Polycythemia Vera
1y57_a P12931 ENSG00000197122 SRC 99.10 3.00E-15 3.90E-19 150.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
BRAF BRAF1 RAFB1
Serine/threonine-protein kinase B-raf (EC 2.7.11.1) (Proto-oncogene B-Raf) (p94) (v-Raf murine sarcoma viral oncogene homolog B1)
2.7.11.1 Homo sapiens
Spitzoid Melanoma,Melanoma In Congenital Melanocytic Nevus,Ventricular Septal Defect,Pancreatic Adenocarcinoma,Melanotic Neuroectodermal Tumor,Skin Melanoma,Gliomatosis Cerebri,Endometrial Cancer,Autosomal Dominant Polycystic Kidney Disease,Endosalpingiosis,Follicular Adenoma,Squamous Cell Carcinoma,Brain Stem Glioma,Thyroid Gland Cancer,Lung Cancer Susceptibility 3,Acral Lentiginous Melanoma,Metanephric Adenoma,Pulmonary Valve Stenosis,Primary Mediastinal B-Cell Lymphoma,Polycystic Kidney Disease,Suppression Of Tumorigenicity 12,Melanoma,Leukemia, Chronic Myeloid,Plasma Cell Neoplasm,Erdheim-Chester Disease,Thyroid Gland Anaplastic Carcinoma,Posterior Uveal Melanoma,Adenoma,Amelanotic Melanoma,Granulomatous Dermatitis,Acneiform Dermatitis,Juvenile Xanthogranuloma,Hypertrophic Cardiomyopathy,Childhood Pilocytic Astrocytoma,Rasopathy,Nonseminomatous Germ Cell Tumor,Desmoplastic Infantile Astrocytoma,Desmoplastic Infantile Ganglioglioma,Tall Cell Variant Papillary Carcinoma,Refractory Hairy Cell Leukemia,Refractory Hematologic Cancer,Costello Syndrome,Astroblastoma,Differentiated Thyroid Carcinoma,Eosinophilic Cystitis,Familial Colorectal Cancer,Leukemia,Colon Adenocarcinoma,Colonic Benign Neoplasm,Pilomyxoid Astrocytoma,Cerebellar Astrocytoma,Pilocytic Astrocytoma,Pleomorphic Xanthoastrocytoma,Pilocytic Astrocytoma Of Cerebellum,Diffuse Astrocytoma,Serrated Polyposis Syndrome,Pseudo-Turner Syndrome,Arteriovenous Malformations Of The Brain,Wilms Tumor 5,Glioma,Noonan Syndrome 1,Newborn Respiratory Distress Syndrome,Respiratory Distress Syndrome, Infant,Rhabdoid Meningioma,Noonan Syndrome And Noonan-Related Syndrome,Ganglioglioma,Neuronal Tumor,Desmoplastic Infantile Astrocytoma/Ganglioglioma,Papillary Tumor Of The Pineal Region,Dandy-Walker Syndrome,Struma Ovarii,Transitional Cell Carcinoma,Rosai-Dorfman Disease,Classic Hairy Cell Leukemia,Adenofibroma,Benign Struma Ovarii,Thyroid Carcinoma,Nodular Malignant Melanoma,Bladder Cancer,Thyroid Tumor,Brain Cancer,Spitz Nevus,Nodular Goiter,Testicular Germ Cell Tumor,Hairy Cell Leukemia,Lip Cancer,Syringocystadenoma Papilliferum,Lip And Oral Cavity Cancer,Mature Teratoma,Ovarian Cancer,Nevus Of Ota,Adenocarcinoma,Myopericytoma,Urachal Adenocarcinoma,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Malignant Astrocytoma,High Grade Glioma,Gliosarcoma,Giant Cell Glioblastoma,Juvenile Astrocytoma,Colorectal Cancer,Ovarian Serous Cystadenocarcinoma,Cystadenocarcinoma,Papillary Carcinoma,Serous Cystadenocarcinoma,Hepatocellular Carcinoma,Skin Squamous Cell Carcinoma,Skin Benign Neoplasm,Verrucous Papilloma,Cardiofaciocutaneous Syndrome 1,Tethered Spinal Cord Syndrome,Cardiomyopathy, Familial Hypertrophic, 4,Noonan Syndrome With Multiple Lentigines,Sarcoma,Hypothyroidism,Histiocytosis,Skin Carcinoma,Gastric Cancer,Prostate Cancer,Papillary Thyroid Microcarcinoma,Cholangiocarcinoma,Noonan Syndrome 7,Leopard Syndrome 3,Panniculitis,Adrenal Cortical Carcinoma,Ovary Adenocarcinoma,Gastric Adenocarcinoma,Nephrotic Syndrome, Type 3,Craniopharyngioma,Melphalan Allergy,Papillary Craniopharyngioma,Lynch Syndrome,Apocrine Adenoma,Lung Squamous Cell Carcinoma,Adrenal Carcinoma,Thyroid Gland Follicular Carcinoma,Langerhans Cell Histiocytosis,Thyroid Gland Papillary Carcinoma,Bladder Urothelial Carcinoma,Lymphoma, Non-Hodgkin, Familial,Renal Cell Carcinoma, Papillary, 1,Thyroid Cancer, Nonmedullary, 2,Thyroid Cancer, Nonmedullary, 1,Phace Association,Colorectal Cancer, Hereditary Nonpolyposis, Type 5,Hashimoto Thyroiditis,Gastrointestinal Stromal Tumor,Colorectal Adenocarcinoma,Villous Adenoma,Renal Cell Carcinoma, Nonpapillary,Mucosal Melanoma,Wilms Tumor 1,Hypertelorism,Lymphoma,Colitis,Lentigines,Leopard Syndrome 1,Leukemia, Chronic Lymphocytic,Juvenile Myelomonocytic Leukemia,Myeloma, Multiple,Melanoma, Cutaneous Malignant 1,Melanoma, Uveal,Lung Cancer,Pancreatic Cancer,Multiple Pterygium Syndrome, Escobar Variant,Pulmonic Stenosis
4h58_c P15056 ENSG00000157764 BRAF 99.20 2.20E-15 3.00E-19 138.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 4.80E-15 6.10E-19 145.90 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 5.90E-15 7.60E-19 144.90 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
EIF2AK2 PKR PRKR
Interferon-induced, double-stranded RNA-activated protein kinase (EC 2.7.11.1) (Eukaryotic translation initiation factor 2-alpha kinase 2) (eIF-2A protein kinase 2) (Interferon-inducible RNA-dependent protein kinase) (P1/eIF-2A protein kinase) (Protein kinase RNA-activated) (PKR) (Protein kinase R) (Tyrosine-protein kinase EIF2AK2) (EC 2.7.10.2) (p68 kinase)
2.7.10.2,2.7.11.1, Homo sapiens
Human Herpesvirus 8,Hepatitis C,Melanoma,Viral Infectious Disease,Hepatitis D,Alzheimer Disease,Stomatitis,Hepatitis,Acute Leukemia,Influenza,Chronic Fatigue Syndrome,Mumps,Rift Valley Fever,Herpes Simplex,Newcastle Disease,Measles,Hepatitis C Virus,Vaccinia,Fanconi Anemia, Complementation Group C,Creutzfeldt-Jakob Disease,Immune Deficiency Disease,Dystonia 16,Leukoencephalopathy, Developmental Delay, And Episodic Neurologic Regression Syndrome,Microphthalmia With Limb Anomalies,Lung Cancer
2a19_b P19525 ENSG00000055332 EIF2AK2 99.20 5.40E-16 7.60E-20 142.40 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 3.90E-15 4.90E-19 147.70 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
FGFR2 BEK KGFR KSAM
Fibroblast growth factor receptor 2 (FGFR-2) (EC 2.7.10.1) (K-sam) (KGFR) (Keratinocyte growth factor receptor) (CD antigen CD332)
2.7.10.1 Homo sapiens
Bone Disease,Acanthosis Nigricans,Bone Development Disease,Achondroplasia,Physical Disorder,Uterine Carcinosarcoma,Endometrial Cancer,Apert Syndrome,Clear Cell Acanthoma,Autosomal Dominant Polycystic Kidney Disease,Saethre-Chotzen Syndrome,Acanthoma,Squamous Cell Carcinoma,Pfeiffer Syndrome,Lung Cancer Susceptibility 3,Calcinosis,Polycystic Kidney Disease,Pleuropulmonary Blastoma,Acne,Dysostosis,Exophthalmos,Familial Scaphocephaly Syndrome,Exposure Keratitis,Synostosis,Dysgerminoma,Skin Tag,Rasopathy,Deafness, Autosomal Recessive 71,Ectodermal Dysplasia,Brachyolmia Type 4 With Mild Epiphyseal And Metaphyseal Changes,Holoprosencephaly,Split Hand-Foot Malformation,Ankylosis,Cervical Keratinizing Squamous Cell Carcinoma,Radioulnar Synostosis,Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate,Plagiocephaly,Syndromic Craniosynostosis,Craniosynostosis,Chronic Inflammation Of Lacrimal Passage,Dacryocystocele,Bile Duct Adenocarcinoma,Esophagus Adenocarcinoma,Nevus, Epidermal,Luteoma,Testicular Spermatocytic Seminoma,Intrahepatic Cholangiocarcinoma,Glioma,Fibrolamellar Carcinoma,Hepatocellular Clear Cell Carcinoma,Cytochrome P450 Oxidoreductase Deficiency,Fgfr Craniosynostosis Syndromes,Bladder Cancer,Pigmentation Disease,Wolffian Duct Adenocarcinoma,Osteoglophonic Dysplasia,Endometrial Adenocarcinoma,Adult Teratoma,Ovarian Cancer,Adenocarcinoma,Eccrine Papillary Adenocarcinoma,Breast Cancer,Glioblastoma,Wells Syndrome,Colorectal Cancer,Hypospadias,Hydrocephalus,Cholesteatoma Of Middle Ear,Scaphocephaly, Maxillary Retrusion, And Mental Retardation,Muenke Syndrome,Syringomyelia,Myxoid Liposarcoma,Van Der Woude Syndrome 1,Cleft Palate, Isolated,Cleidocranial Dysplasia,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Cholangiocarcinoma,Craniosynostosis 1,Jackson-Weiss Syndrome,Kallmann Syndrome,Crouzon Syndrome,Beare-Stevenson Cutis Gyrata Syndrome,Skin Disease,Gastric Adenocarcinoma,Porokeratosis,Aplasia Of Lacrimal And Salivary Glands,Lung Squamous Cell Carcinoma,Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1,Hydrocephalus, Congenital, 1,Antley-Bixler Syndrome,Split-Hand/Foot Malformation 1,Esophageal Cancer,Hypertelorism, Microtia, Facial Clefting Syndrome,Odontochondrodysplasia,Orofacial Cleft,Strabismus,Hemifacial Hyperplasia,Chromosome 2q35 Duplication Syndrome,Tooth Agenesis,Thanatophoric Dysplasia, Type I,Renal Hypodysplasia/Aplasia 1,Humeroradial Synostosis,Vesicoureteral Reflux 1,Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans,Nasopharyngeal Carcinoma,Bent Bone Dysplasia Syndrome,Hypertelorism,Hypochondroplasia,Estrogen-Receptor Positive Breast Cancer,Carpenter Syndrome 1,Lacrimoauriculodentodigital Syndrome,Scoliosis,Antley-Bixler Syndrome Without Genital Anomalies Or Disordered Steroidogenesis,Chromosomal Duplication Syndrome,Lung Cancer,Pancreatic Cancer,Peters-Plus Syndrome,Multiple Pterygium Syndrome, Escobar Variant
2psq_a P21802 ENSG00000066468 FGFR2 99.20 1.60E-15 2.20E-19 148.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
ERBB3 HER3
Receptor tyrosine-protein kinase erbB-3 (EC 2.7.10.1) (Proto-oncogene-like protein c-ErbB-3) (Tyrosine kinase-type cell surface receptor HER3)
2.7.10.1 Homo sapiens
Pancreatic Adenocarcinoma,Uterine Carcinosarcoma,Lung Cancer Susceptibility 3,Clear Cell Sarcoma,Mucinous Lung Adenocarcinoma,Neurogenic Bladder,Acute Erythroid Leukemia,Leukemia,Colonic Benign Neoplasm,Pilocytic Astrocytoma,Acoustic Neuroma,Periampullary Adenocarcinoma,Keratoconjunctivitis Sicca,Transitional Cell Carcinoma,Bladder Cancer,Retroperitoneal Leiomyosarcoma,Paronychia,Mixed Cell Adenoma,Vallecula Cancer,Ovarian Cancer,Gastric Fundus Cancer,Adenocarcinoma,Charcot-Marie-Tooth Disease,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Colorectal Cancer,Squamous Blepharitis,Gallbladder Cancer,Tooth Disease,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Cervical Cancer,Gastric Adenocarcinoma,Verrucous Carcinoma,Childhood Medulloblastoma,Schizophrenia,Ovary Transitional Cell Carcinoma,Bladder Urothelial Carcinoma,Erythroleukemia, Familial,Esophageal Cancer,Ductal Carcinoma In Situ,Estrogen-Receptor Positive Breast Cancer,Lethal Congenital Contracture Syndrome 2,Lethal Congenital Contracture Syndrome 1,Medulloblastoma,Lethal Congenital Contracture Syndrome,Lung Cancer,Pancreatic Cancer
3kex_a P21860 ENSG00000065361 ERBB3 99.20 2.70E-15 3.50E-19 143.70 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.20 2.10E-15 2.80E-19 147.40 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
FGFR4 JTK2 TKF
Fibroblast growth factor receptor 4 (FGFR-4) (EC 2.7.10.1) (CD antigen CD334)
2.7.10.1 Homo sapiens
Functional Diarrhea,Gliomatosis Cerebri,Squamous Cell Carcinoma,Lung Cancer Susceptibility 3,Neuroendocrine Carcinoma,Adenoid Cystic Carcinoma,Rhabdomyosarcoma 2,Neuroma,Outlet Dysfunction Constipation,Constipation,Craniosynostosis,Nevus, Epidermal,Frontal Convexity Meningioma,Leber Plus Disease,Hepatocellular Clear Cell Carcinoma,Soft Tissue Sarcoma,Adenocarcinoma,Breast Cancer,Extrahepatic Cholestasis,Squamous Cell Carcinoma, Head And Neck,Anaplastic Astrocytoma,Colorectal Cancer,Hepatocellular Carcinoma,Rhabdomyosarcoma,Orbit Embryonal Rhabdomyosarcoma,Orbit Rhabdomyosarcoma,Prostate Cancer,Crouzon Syndrome,Lung Squamous Cell Carcinoma,Skeletal Muscle Cancer,Muscle Cancer,Odontochondrodysplasia,Thanatophoric Dysplasia, Type I,Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans,Hypochondroplasia,Hypophosphatemic Rickets, X-Linked Dominant,Lacrimoauriculodentodigital Syndrome,Parameningeal Embryonal Rhabdomyosarcoma,Pancreatic Cancer,Bjornstad Syndrome
6jpj_a P22455 ENSG00000160867 FGFR4 99.20 2.30E-15 3.10E-19 141.80 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 3.30E-15 4.30E-19 144.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
JAK1 JAK1A JAK1B
Tyrosine-protein kinase JAK1 (EC 2.7.10.2) (Janus kinase 1) (JAK-1)
2.7.10.2 Homo sapiens
Psoriasis,Breast Implant-Associated Anaplastic Large Cell Lymphoma,Endometrial Cancer,Severe Combined Immunodeficiency,Hepatitis C,Covid-19,Blood Platelet Disease,Hepatitis,Leukemia,Blood Coagulation Disease,Wernicke Encephalopathy,Leukemia, Acute Myeloid,Sting-Associated Vasculopathy With Onset In Infancy,Bone Marrow Cancer,Leukemia, Acute Lymphoblastic,Combined Immunodeficiency,Polycythemia,Autosomal Recessive Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Jak1 Deficiency,Crisponi/Cold-Induced Sweating Syndrome 1,Colonic Disease,Acute Megakaryoblastic Leukemia In Down Syndrome,Herpes Zoster,Autoimmune Lymphoproliferative Syndrome,T-Cell Prolymphocytic Leukemia,Mixed Lacrimal Gland Cancer,Prolymphocytic Leukemia,Nasopharyngitis,Ovarian Cancer,T-Cell Acute Lymphoblastic Leukemia,Acute Megakaryocytic Leukemia,Breast Cancer,Colorectal Cancer,Hepatocellular Carcinoma,Jak3-Deficient Severe Combined Immunodeficiency,Fibrosarcoma,Prostate Cancer,Chilblain Lupus 1,Severe Combined Immunodeficiency, X-Linked,Mouth Disease,Immunodeficiency 27b,Immunodeficiency 35,Aicardi-Goutieres Syndrome,Down Syndrome,Acute Promyelocytic Leukemia,Lymphoblastic Leukemia, Acute, With Lymphomatous Features,Leukemia, Acute, X-Linked,Alopecia Universalis Congenita,Autoinflammation, Immune Dysregulation, And Eosinophilia,Systemic Lupus Erythematosus,Myelofibrosis,Lymphoproliferative Syndrome,Immunodeficiency 27a,Pancreatic Cancer,Polycythemia Vera
3eyh_a P23458 ENSG00000162434 JAK1 99.20 1.90E-15 2.70E-19 139.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 6.90E-15 8.90E-19 144.10 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
PRKACA
cAMP-dependent protein kinase catalytic subunit alpha (PKA C-alpha) (EC 2.7.11.11)
2.7.11.11 Cricetulus griseus
5n3j_a P25321 99.10 5.60E-15 7.20E-19 145.20 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
HRR25 YPL204W
Casein kinase I homolog HRR25 (EC 2.7.11.1)
2.7.11.1 Saccharomyces cerevisiae
5czo_b P29295 99.10 6.60E-15 8.40E-19 147.20 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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
2qoc_a P29320 ENSG00000044524 EPHA3 99.10 6.90E-15 8.90E-19 143.20 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
AXL UFO
Tyrosine-protein kinase receptor UFO (EC 2.7.10.1) (AXL oncogene)
2.7.10.1 Homo sapiens
Ocular Melanoma,Retinitis Pigmentosa,Leukemia, Chronic Myeloid,Diabetes Mellitus,Clear Cell Renal Cell Carcinoma,Lymphocytic Choriomeningitis,Mesangial Proliferative Glomerulonephritis,Leukemia, Acute Myeloid,Congenital Disorder Of Glycosylation, Type Il,Borna Disease,Fundus Dystrophy,Nk-Cell Enteropathy,Adenocarcinoma,Breast Cancer,Renal Cell Carcinoma, Papillary, 1,Renal Cell Carcinoma, Nonpapillary,Hypogonadotropic Hypogonadism 7 With Or Without Anosmia,Zika Fever,Lung Cancer
5u6b_b P30530 ENSG00000167601 AXL 99.10 2.70E-15 3.80E-19 140.10 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.20 2.60E-15 3.40E-19 146.80 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 6.50E-15 9.20E-19 133.90 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
KDR FLK1 VEGFR2
Vascular endothelial growth factor receptor 2 (VEGFR-2) (EC 2.7.10.1) (Fetal liver kinase 1) (FLK-1) (Kinase insert domain receptor) (KDR) (Protein-tyrosine kinase receptor flk-1) (CD antigen CD309)
2.7.10.1 Homo sapiens
Psoriasis,Pancreatic Adenocarcinoma,Corneal Neovascularization,Mesothelioma, Malignant,Skin Melanoma,Pneumothorax,Heart Disease,Neovascular Glaucoma,Endocrine Gland Cancer,Retinal Vein Occlusion,Retinal Vascular Occlusion,Vascular Cancer,Retinitis Pigmentosa,Thyroid Gland Cancer,Ovarian Hyperstimulation Syndrome,Lung Cancer Susceptibility 3,Chronic Myelomonocytic Leukemia,Bone Cancer,Microvascular Complications Of Diabetes 5,Mast-Cell Leukemia,Melanoma,Malignant Ciliary Body Melanoma,Lung Non-Squamous Non-Small Cell Carcinoma,Diabetes Mellitus,Degeneration Of Macula And Posterior Pole,Macular Retinal Edema,Clear Cell Renal Cell Carcinoma,Septate Uterus,Primary Cutaneous B-Cell Lymphoma,Myocardial Infarction,Breast Angiosarcoma,Eye Degenerative Disease,Placenta Accreta,Cavernous Hemangioma,Neuroblastoma,Pilocytic Astrocytoma,Epithelioid Hemangioendothelioma,Arteriovenous Malformations Of The Brain,Olecranon Bursitis,Pulmonary Vein Stenosis,Retinal Vascular Disease,Gastroesophageal Junction Adenocarcinoma,Leukemia, Acute Myeloid,Capillary Disease,Hematologic Cancer,Hemangioma,Radiation Proctitis,Kidney Cancer,Leukostasis,Aortic Valve Disease 1,Hemangioblastoma,Bladder Cancer,Capillary Hemangioma,Heritable Pulmonary Arterial Hypertension,Retinal Artery Occlusion,Fundus Dystrophy,Parasitic Protozoa Infectious Disease,Kaposiform Hemangioendothelioma,Nodular Goiter,Background Diabetic Retinopathy,Endometriosis,Pediculus Humanus Capitis Infestation,Vein Disease,Bursitis,Ovarian Cancer,Hemangioma, Capillary Infantile,Adenocarcinoma,Pre-Eclampsia,Eye Disease,Cervical Adenosquamous Carcinoma,Breast Carcinoma In Situ,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Rosacea,High Grade Glioma,Gliosarcoma,Colorectal Cancer,Familial Hypercholesterolemia,Hepatocellular Carcinoma,Proctitis,Premature Menopause,8p11 Myeloproliferative Syndrome,Clopidogrel Resistance,Kuhnt-Junius Degeneration,Angiokeratoma Of Mibelli,Angiokeratoma Circumscriptum,Pheochromocytoma,Rhabdomyosarcoma,Ischemia,Cerebral Cavernous Malformations,Conjunctival Vascular Disease,Macular Degeneration, Age-Related, 1,Sarcoma,Hantavirus Pulmonary Syndrome,Fibrosarcoma Of Bone,Skin Carcinoma,Gastric Cancer,Lymphangioma,Mobitz Type Ii Atrioventricular Block,Prostate Cancer,Disease Of Mental Health,Coats Disease,Microvascular Complications Of Diabetes 1,Pulmonary Hypertension,Type 2 Diabetes Mellitus,Angiosarcoma,Drug-Induced Lupus Erythematosus,Placental Insufficiency,Thyroid Gland Follicular Carcinoma,Merkel Cell Carcinoma,Thyroid Gland Medullary Carcinoma,Renal Cell Carcinoma, Papillary, 1,Esophageal Cancer,Exudative Vitreoretinopathy 1,Tetralogy Of Fallot,Myelodysplastic Syndrome,Sorsby Fundus Dystrophy,Ewing Sarcoma,Gastrointestinal Stromal Tumor,Varicose Veins,Hirschsprung Disease 1,Limb Ischemia,Bone Squamous Cell Carcinoma,Renal Cell Carcinoma, Nonpapillary,Mucosal Melanoma,Hypertension, Essential,Lipoprotein Quantitative Trait Locus,Cardiovascular Organ Benign Neoplasm,Intussusception,Moyamoya Disease 1,Premature Ovarian Failure 1,Medulloblastoma,Lung Cancer,Pancreatic Cancer
4ase_a P35968 ENSG00000128052 KDR 99.20 1.50E-15 2.00E-19 147.90 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
Btk Bpk
Tyrosine-protein kinase BTK (EC 2.7.10.2) (Agammaglobulinemia tyrosine kinase) (ATK) (B-cell progenitor kinase) (BPK) (Bruton tyrosine kinase) (Kinase EMB)
2.7.10.2 Mus musculus
4xi2_a P35991 99.20 1.50E-15 2.00E-19 153.00 0 0 1 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
TGFBR1 ALK5 SKR4
TGF-beta receptor type-1 (TGFR-1) (EC 2.7.11.30) (Activin A receptor type II-like protein kinase of 53kD) (Activin receptor-like kinase 5) (ALK-5) (ALK5) (Serine/threonine-protein kinase receptor R4) (SKR4) (TGF-beta type I receptor) (Transforming growth factor-beta receptor type I) (TGF-beta receptor type I) (TbetaR-I)
2.7.11.30 Homo sapiens
Endometrial Cancer,Transient Hypogammaglobulinemia Of Infancy,Transient Hypogammaglobulinemia,Loeys-Dietz Syndrome 4,Endometrial Stromal Sarcoma,Mitochondrial Dna Depletion Syndrome 12b,Connective Tissue Disease,Acantholytic Acanthoma,Aortic Dissection,Familial Colorectal Cancer,Pulsating Exophthalmos,Familial Thoracic Aortic Aneurysm And Aortic Dissection,Craniosynostosis,Hereditary Hemorrhagic Telangiectasia,Telangiectasis,Classic Ehlers-Danlos Syndrome,Aortic Disease,Aortic Valve Disease 1,Bladder Cancer,Heritable Thoracic Aortic Disease,Collagen Disease,Ehlers-Danlos Syndrome,Osteoporosis,Ovarian Cancer,Loeys-Dietz Syndrome 1,Tricuspid Valve Prolapse,Breast Cancer,Squamous Cell Carcinoma, Head And Neck,Aortic Valve Insufficiency,Colorectal Cancer,Hepatocellular Carcinoma,Aneurysm,Frozen Shoulder,Intracranial Aneurysm,Juvenile Polyposis/Hereditary Hemorrhagic Telangiectasia Syndrome,Cleft Palate, Isolated,Gastric Cancer,Loeys-Dietz Syndrome 5,Arteriovenous Malformation,Loeys-Dietz Syndrome 2,Prostate Cancer,Pulmonary Hypertension,Cutis Laxa, Autosomal Dominant 1,Aortic Aneurysm,Pulmonary Fibrosis, Idiopathic,Loeys-Dietz Syndrome 3,Orthostatic Intolerance,Ehlers-Danlos Syndrome, Classic Type, 1,Camurati-Engelmann Disease,Loeys-Dietz Syndrome,Multiple Self-Healing Squamous Epithelioma,Aortic Aneurysm, Familial Thoracic 4,Orofacial Cleft,Aortic Aneurysm, Familial Thoracic 6,Renal Fibrosis,Aortic Aneurysm, Familial Thoracic 1,Cutaneous T Cell Lymphoma,Patent Ductus Arteriosus 1,Keloid Formation,Arterial Tortuosity Syndrome,Marfan Syndrome,Marfanoid Hypermobility Syndrome,Lung Cancer,Pancreatic Cancer
5e8x_a P36897 ENSG00000106799 TGFBR1 99.10 6.10E-15 8.50E-19 137.70 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 5.20E-15 6.80E-19 143.30 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
CSNK1D HCKID
Casein kinase I isoform delta (CKI-delta) (CKId) (EC 2.7.11.1) (Tau-protein kinase CSNK1D) (EC 2.7.11.26)
2.7.11.1,2.7.11.26, Homo sapiens
Migraine With Or Without Aura 1,Alzheimer Disease,Sleep Disorder,Advanced Sleep Phase Syndrome, Familial, 2,Breast Cancer,Disease Of Mental Health,Delayed Sleep Phase Disorder,Advanced Sleep Phase Syndrome
6gzm_a P48730 ENSG00000141551 CSNK1D 99.20 1.10E-15 1.50E-19 142.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 4.60E-15 6.00E-19 144.10 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
JAK3
Tyrosine-protein kinase JAK3 (EC 2.7.10.2) (Janus kinase 3) (JAK-3) (Leukocyte janus kinase) (L-JAK)
2.7.10.2 Homo sapiens
Lymphopenia,Reticular Dysgenesis,Severe Combined Immunodeficiency,Myeloproliferative Syndrome, Transient,Common Variable Immunodeficiency,Myeloproliferative Neoplasm,Leukemia,Childhood Leukemia,Leukemia, Acute Myeloid,Leukemia, Acute Lymphoblastic,Combined Immunodeficiency,Autoimmune Disease,T-B- Severe Combined Immunodeficiency,Geotrichosis,Sezary'S Disease,T-Cell Prolymphocytic Leukemia,Prolymphocytic Leukemia,Nk-Cell Enteropathy,T-Cell Adult Acute Lymphocytic Leukemia,T-Cell Acute Lymphoblastic Leukemia,Acute Megakaryocytic Leukemia,Adenosine Deaminase Deficiency,Jak3-Deficient Severe Combined Immunodeficiency,Alk-Positive Anaplastic Large Cell Lymphoma,Hyper Ige Recurrent Infection Syndrome 1,Chronic Granulomatous Disease,Omenn Syndrome,Severe Combined Immunodeficiency, X-Linked,Adult T-Cell Leukemia,Immunodeficiency 35,Immune Deficiency Disease,Immunodeficiency 63 With Lymphoproliferation And Autoimmunity,Mature T-Cell And Nk-Cell Lymphoma,Anaplastic Large Cell Lymphoma,Peripheral T-Cell Lymphoma,Down Syndrome,Lymphoblastic Leukemia, Acute, With Lymphomatous Features,Bone Squamous Cell Carcinoma,Janus Kinase-3 Deficiency,Cd40 Ligand Deficiency,Jacobsen Syndrome,Alopecia Universalis Congenita,Juvenile Myelomonocytic Leukemia,Myelofibrosis,Bare Lymphocyte Syndrome, Type Ii,Lung Cancer,Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative,Polycythemia Vera
1yvj_a P52333 ENSG00000105639 JAK3 99.10 3.20E-15 4.40E-19 138.10 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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
2x0g_a P53355 ENSG00000196730 DAPK1 99.20 2.50E-15 3.20E-19 146.20 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 4.80E-15 6.50E-19 137.30 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
EPHB4 HTK MYK1 TYRO11
Ephrin type-B receptor 4 (EC 2.7.10.1) (Hepatoma transmembrane kinase) (Tyrosine-protein kinase TYRO11)
2.7.10.1 Homo sapiens
Endometrial Cancer,Liver Carcinoma In Situ,Capillary Malformation-Arteriovenous Malformation 1,Skin Angiosarcoma,Parkes Weber Syndrome,Brain Stem Astrocytic Neoplasm,Hereditary Hemorrhagic Telangiectasia,Lymphatic Malformation 7,Ovarian Cancer,Breast Cancer,Squamous Cell Carcinoma, Head And Neck,Weber Syndrome,Colorectal Cancer,Arteriovenous Malformation,Microvascular Complications Of Diabetes 1,Capillary Malformation-Arteriovenous Malformation 2,Tetralogy Of Fallot,Cardiovascular Organ Benign Neoplasm,Hennekam Syndrome
6fnk_a P54760 ENSG00000196411 EPHB4 99.10 5.00E-15 6.80E-19 139.00 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
Tyro3 Dtk Rse Tif
Tyrosine-protein kinase receptor TYRO3 (EC 2.7.10.1) (Etk2/tyro3) (TK19-2) (Tyrosine-protein kinase DTK) (Tyrosine-protein kinase RSE) (Tyrosine-protein kinase TIF)
2.7.10.1 Mus musculus
3qup_a P55144 99.20 2.20E-15 3.00E-19 143.70 0 0 1 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
MAP3K9 MLK1 PRKE1
Mitogen-activated protein kinase kinase kinase 9 (EC 2.7.11.25) (Mixed lineage kinase 1)
2.7.11.25 Homo sapiens
Ecthyma,Esophagus Squamous Cell Carcinoma,Retroperitoneal Neuroblastoma
4uy9_b P80192 ENSG00000006432 MAP3K9 99.10 3.00E-15 4.00E-19 143.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
pknE Rv1743 MTCY28.05
Serine/threonine-protein kinase PknE (EC 2.7.11.1)
2.7.11.1 Mycobacterium tuberculosis
2h34_a P9WI77 99.10 6.50E-15 8.50E-19 140.80 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
pknB Rv0014c MTCY10H4.14c
Serine/threonine-protein kinase PknB (EC 2.7.11.1)
2.7.11.1 Mycobacterium tuberculosis
6i2p_a P9WI81 99.10 3.90E-15 5.40E-19 136.30 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
pknA Rv0015c MTCY10H4.15c
Serine/threonine-protein kinase PknA (EC 2.7.11.1)
2.7.11.1 Mycobacterium tuberculosis
4ow8_a P9WI83 99.10 4.70E-15 6.50E-19 136.90 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
PTK2 FAK FAK1
Focal adhesion kinase 1 (FADK 1) (EC 2.7.10.2) (Focal adhesion kinase-related nonkinase) (FRNK) (p41/p43FRNK) (Protein-tyrosine kinase 2) (p125FAK) (pp125FAK)
2.7.10.2 Gallus gallus
2j0l_a Q00944 99.10 4.80E-15 6.70E-19 136.30 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
ROR2 NTRKR2
Tyrosine-protein kinase transmembrane receptor ROR2 (EC 2.7.10.1) (Neurotrophic tyrosine kinase, receptor-related 2)
2.7.10.1 Homo sapiens
Robinow Syndrome, Autosomal Recessive 1,Autosomal Dominant Robinow Syndrome,Basal Cell Nevus Syndrome,Brachydactyly, Type A1,Ror2-Related Robinow Syndrome,Brachydactyly, Type B1,Fallopian Tube Serous Adenocarcinoma,Breast Cancer,Polydactyly,Robinow Syndrome, Autosomal Dominant 1,Brachydactyly,Distal Arthrogryposis,Proximal Symphalangism,Robinow Syndrome,Omodysplasia,Fetal Akinesia Deformation Sequence 1
3zzw_a Q01974 ENSG00000169071 ROR2 99.20 2.60E-15 3.70E-19 137.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
PRKCQ PRKCT
Protein kinase C theta type (EC 2.7.11.13) (nPKC-theta)
2.7.11.13 Homo sapiens
Inflammatory Bowel Disease 1,T-Cell Lymphoblastic Leukemia/Lymphoma,Crohn'S Disease,Breast Cancer,Gastrointestinal Stromal Tumor
4ra5_a Q04759 ENSG00000065675 PRKCQ 99.10 4.10E-15 5.30E-19 144.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
ACVR1 ACVRLK2
Activin receptor type-1 (EC 2.7.11.30) (Activin receptor type I) (ACTR-I) (Activin receptor-like kinase 2) (ALK-2) (Serine/threonine-protein kinase receptor R1) (SKR1) (TGF-B superfamily receptor type I) (TSR-I)
2.7.11.30 Homo sapiens
Brain Stem Glioma,Brain Stem Cancer,Childhood Brain Stem Glioma,Double Outlet Right Ventricle,Myositis Ossificans,Diffuse Midline Glioma, H3 K27m-Mutant,Heel Spur,Myositis,Ankylosis,Chronic Pulmonary Heart Disease,Hemochromatosis Type 2,Brachydactyly, Type A1, C,High-Grade Astrocytoma,Microphthalmia, Isolated 4,Aortic Valve Disease 1,Brachydactyly, Type A2,Osseous Heteroplasia, Progressive,High Grade Glioma,Juvenile Polyposis/Hereditary Hemorrhagic Telangiectasia Syndrome,Brittle Bone Disorder,Craniometaphyseal Dysplasia, Autosomal Dominant,Pulmonary Hypertension,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Gastric Adenocarcinoma,Brachydactyly, Type B2,Odontochondrodysplasia,Fibrodysplasia Ossificans Progressiva,Synostoses, Tarsal, Carpal, And Digital,Tarsal-Carpal Coalition Syndrome,Atrioventricular Septal Defect,Proximal Symphalangism,Persistent Mullerian Duct Syndrome,Brachydactyly, Type A1, B
3q4u_c Q04771 ENSG00000115170 ACVR1 99.10 4.00E-15 5.60E-19 137.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.20 4.80E-16 6.50E-20 144.40 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
TNK2 ACK1
Activated CDC42 kinase 1 (ACK-1) (EC 2.7.10.2) (EC 2.7.11.1) (Tyrosine kinase non-receptor protein 2)
2.7.10.2 Homo sapiens
Gastric Cardia Carcinoma,Epilepsy,Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression,Parkinson Disease, Late-Onset
4ewh_a Q07912 ENSG00000061938 TNK2 99.10 2.80E-15 3.90E-19 137.00 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
DDR1 CAK EDDR1 NEP NTRK4 PTK3A RTK6 TRKE
Epithelial discoidin domain-containing receptor 1 (Epithelial discoidin domain receptor 1) (EC 2.7.10.1) (CD167 antigen-like family member A) (Cell adhesion kinase) (Discoidin receptor tyrosine kinase) (HGK2) (Mammary carcinoma kinase 10) (MCK-10) (Protein-tyrosine kinase 3A) (Protein-tyrosine kinase RTK-6) (TRK E) (Tyrosine kinase DDR) (Tyrosine-protein kinase CAK) (CD antigen CD167a)
2.7.10.1 Homo sapiens
Cervix Small Cell Carcinoma,Meninges Sarcoma,Breast Cancer,Alport Syndrome,Pulmonary Fibrosis, Idiopathic,Lymphangioleiomyomatosis
3zos_b Q08345 ENSG00000204580 DDR1 99.10 4.60E-15 6.10E-19 141.80 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
ITK EMT LYK
Tyrosine-protein kinase ITK/TSK (EC 2.7.10.2) (Interleukin-2-inducible T-cell kinase) (IL-2-inducible T-cell kinase) (Kinase EMT) (T-cell-specific kinase) (Tyrosine-protein kinase Lyk)
2.7.10.2 Homo sapiens
Lymphopenia,Allergic Asthma,B Cell Deficiency,Pancytopenia,Angioimmunoblastic T-Cell Lymphoma,Mixed Oligodendroglioma-Astrocytoma,Lymphoproliferative Syndrome 1,Agammaglobulinemia,Lymphoproliferative Syndrome 2,Epidermodysplasia Verruciformis 1,Cone-Rod Dystrophy 2,Disease Of Mental Health,Immunodeficiency 17,Thrombocytopenia,Hemophagocytic Lymphohistiocytosis,Lymphoproliferative Syndrome, X-Linked, 2,Agammaglobulinemia, X-Linked,Immunodeficiency, X-Linked, With Magnesium Defect, Epstein-Barr Virus Infection, And Neoplasia,Peripheral T-Cell Lymphoma,Epilepsy, Familial Temporal Lobe, 8,Coronin-1a Deficiency,Lymphoproliferative Syndrome, X-Linked, 1,Lymphoproliferative Syndrome,Asthma
4hct_a Q08881 ENSG00000113263 ITK 99.10 2.80E-15 3.80E-19 137.00 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
DMPK DM1PK MDPK
Myotonin-protein kinase (MT-PK) (EC 2.7.11.1) (DM-kinase) (DMK) (DM1 protein kinase) (DMPK) (Myotonic dystrophy protein kinase)
2.7.11.1 Homo sapiens
Muscular Disease,Fuchs' Endothelial Dystrophy,Myopathy,Muscle Tissue Disease,Neuromuscular Disease,Hypertrophic Cardiomyopathy,Myotonic Disease,Myotonic Dystrophy 1,Muscular Dystrophy,Myotonic Dystrophy,Spinocerebellar Ataxia 8,Myotonic Cataract,Cataract,Oculopharyngeal Muscular Dystrophy,Hair Follicle Neoplasm,Myotonic Dystrophy 2,Myotonia,Immature Cataract,Lens Disease,Autosomal Dominant Cerebellar Ataxia,Disease Of Mental Health,Fragile X Syndrome,Huntington Disease-Like 2,First-Degree Atrioventricular Block,Fragile X-Associated Tremor/Ataxia Syndrome,X-Linked Hereditary Ataxia,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Catecholaminergic Polymorphic Ventricular Tachycardia,Frontotemporal Dementia,3-Methylglutaconic Aciduria, Type Iii
2vd5_a Q09013 ENSG00000104936 DMPK 99.10 6.70E-15 8.50E-19 147.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 6.60E-15 8.60E-19 143.00 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
ROCK1
Rho-associated protein kinase 1 (EC 2.7.11.1) (Renal carcinoma antigen NY-REN-35) (Rho-associated, coiled-coil-containing protein kinase 1) (Rho-associated, coiled-coil-containing protein kinase I) (ROCK-I) (p160 ROCK-1) (p160ROCK)
2.7.11.1 Homo sapiens
Coronary Artery Vasospasm,Ocular Hyperemia,Breast Cancer,Pediatric Osteosarcoma,Hutchinson-Gilford Progeria Syndrome,Tetralogy Of Fallot,Hypertension, Essential,Lung Cancer
2v55_c Q13464 ENSG00000067900 ROCK1 99.20 2.00E-15 2.40E-19 152.90 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.20 1.70E-15 2.30E-19 146.50 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
PTK6 BRK
Protein-tyrosine kinase 6 (EC 2.7.10.2) (Breast tumor kinase) (Tyrosine-protein kinase BRK)
2.7.10.2 Homo sapiens
Charge Syndrome,Aggressive Systemic Mastocytosis,Breast Cancer,Inclusion Conjunctivitis,Ovary Serous Adenocarcinoma,Thoracic Outlet Syndrome
5d7v_a Q13882 ENSG00000101213 PTK6 99.10 3.10E-15 4.30E-19 137.20 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
PRKG1 PRKG1B PRKGR1A PRKGR1B
cGMP-dependent protein kinase 1 (cGK 1) (cGK1) (EC 2.7.11.12) (cGMP-dependent protein kinase I) (cGKI)
2.7.11.12 Homo sapiens
Myopathy,Impotence,Connective Tissue Disease,Diabetes Mellitus,Aortic Dissection,Alzheimer Disease,Familial Thoracic Aortic Aneurysm And Aortic Dissection,Cystic Fibrosis,Aortic Disease,Aortic Valve Disease 1,Heritable Thoracic Aortic Disease,Hemolytic Anemia,Non-Proliferative Fibrocystic Change Of The Breast,Aneurysm,Aortic Aneurysm, Familial Thoracic 8,Disease Of Mental Health,Pulmonary Hypertension,Body Mass Index Quantitative Trait Locus 11,Aortic Aneurysm,Loeys-Dietz Syndrome,Immune Deficiency Disease,Myelodysplastic Syndrome,Attention Deficit-Hyperactivity Disorder,Aortic Aneurysm, Familial Thoracic 1,Hypertension, Essential,Sexual Disorder
6bg2_a Q13976 ENSG00000185532 PRKG1 99.20 1.70E-15 2.10E-19 149.10 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
PTK2B FAK2 PYK2 RAFTK
Protein-tyrosine kinase 2-beta (EC 2.7.10.2) (Calcium-dependent tyrosine kinase) (CADTK) (Calcium-regulated non-receptor proline-rich tyrosine kinase) (Cell adhesion kinase beta) (CAK-beta) (CAKB) (Focal adhesion kinase 2) (FADK 2) (Proline-rich tyrosine kinase 2) (Related adhesion focal tyrosine kinase) (RAFTK)
2.7.10.2 Homo sapiens
Leukemia, Chronic Myeloid,Transient Cerebral Ischemia,Retinal Degeneration,Mixed Cell Adenoma,Osteoporosis,Ovarian Cancer,Osteopetrosis,Breast Cancer,Hepatocellular Carcinoma,Prostate Cancer,Disease Of Mental Health,Lung Cancer
3cc6_a Q14289 ENSG00000120899 PTK2B 99.20 2.50E-15 3.40E-19 139.20 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 6.30E-15 8.00E-19 144.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.20 2.70E-15 3.50E-19 146.70 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.20 1.80E-15 2.40E-19 146.70 0 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
ROCK2
Rho-associated protein kinase 2 (EC 2.7.11.1) (Rho-associated, coiled-coil-containing protein kinase 2) (Rho-associated, coiled-coil-containing protein kinase II) (ROCK-II) (p164 ROCK-2)
2.7.11.1 Bos taurus
2f2u_b Q28021 99.20 9.20E-16 1.10E-19 155.10 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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
5te0_a Q2M2I8 ENSG00000115977 AAK1 99.20 4.50E-16 5.90E-20 151.90 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
Pto
Pto
Solanum pimpinellifolium
2qkw_b Q40234 99.10 5.70E-15 7.50E-19 141.50 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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
4yfi_a Q59H18 ENSG00000259030 FPGT-TNNI3K 99.30 1.10E-16 1.50E-20 152.30 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
lpl0262
lpl0262
2.7.11.1 Legionella pneumophila
5ckw_b Q5WZW9 99.20 2.60E-15 3.20E-19 154.40 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
Brsk2 Kiaa4256 Sada
Serine/threonine-protein kinase BRSK2 (EC 2.7.11.1) (EC 2.7.11.26) (Brain-specific serine/threonine-protein kinase 2) (BR serine/threonine-protein kinase 2) (Serine/threonine-protein kinase SAD-A)
2.7.11.26 Mus musculus
4ynz_b Q69Z98 99.10 5.20E-15 6.70E-19 144.80 0 0 1 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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
4f1m_a Q6XHB2 99.10 5.80E-15 8.10E-19 135.60 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.20 1.40E-15 1.70E-19 151.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.20 2.30E-15 2.90E-19 149.30 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
NEK7
Serine/threonine-protein kinase Nek7 (EC 2.7.11.1) (Never in mitosis A-related kinase 7) (NimA-related protein kinase 7)
2.7.11.1 Homo sapiens
Erysipeloid
2wqm_a Q8TDX7 ENSG00000151414 NEK7 99.20 2.20E-15 2.90E-19 143.40 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 2.90E-15 3.80E-19 144.90 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
DYRK2
Dual specificity tyrosine-phosphorylation-regulated kinase 2 (EC 2.7.12.1)
2.7.12.1 Homo sapiens
4azf_a Q92630 ENSG00000127334 DYRK2 99.10 6.40E-15 7.90E-19 150.00 0 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
MAP4K1 HPK1
Mitogen-activated protein kinase kinase kinase kinase 1 (EC 2.7.11.1) (Hematopoietic progenitor kinase) (MAPK/ERK kinase kinase kinase 1) (MEK kinase kinase 1) (MEKKK 1)
2.7.11.1 Homo sapiens
6cqd_b Q92918 ENSG00000104814 MAP4K1 99.10 6.40E-15 8.50E-19 138.80 0 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
MAP3K14 NIK
Mitogen-activated protein kinase kinase kinase 14 (EC 2.7.11.25) (NF-kappa-beta-inducing kinase) (HsNIK) (Serine/threonine-protein kinase NIK)
2.7.11.25 Homo sapiens
T-Cell Lymphoblastic Leukemia/Lymphoma,Nik Deficiency,Trichohepatoenteric Syndrome 1,Pancreatic Adenosquamous Carcinoma,Pancreatic Ductal Adenocarcinoma,Immunodeficiency 50
4idv_c Q99558 ENSG00000006062 MAP3K14 99.20 9.90E-16 1.30E-19 149.90 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.20 9.80E-16 1.30E-19 145.90 0 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
CDPK1
CDPK1
Toxoplasma gondii
5t6i_a Q9BJF5 99.10 6.00E-15 7.70E-19 152.50 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.10 3.20E-15 4.00E-19 150.00 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
Ripk4 Ankrd3 Pkk
Receptor-interacting serine/threonine-protein kinase 4 (EC 2.7.11.1) (Ankyrin repeat domain-containing protein 3) (PKC-associated protein kinase) (PKC-regulated protein kinase)
2.7.11.1 Mus musculus
5wnj_a Q9ERK0 99.30 2.20E-16 2.80E-20 154.30 0 0 1 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
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 99.20 2.60E-15 3.40E-19 142.20 0 0 0 0 0 0 1 0
YGR188C BUB1 SGDID:S000003420
CSNK1G1
Casein kinase I isoform gamma-1 (CKI-gamma 1) (EC 2.7.11.1)
2.7.11.1 Homo sapiens
Epilepsy,Epilepsy With Generalized Tonic-Clonic Seizures,Aortic Valve Prolapse,Gm1-Gangliosidosis, Type I,Gm1-Gangliosidosis, Type Ii
2cmw_a Q9HCP0 ENSG00000169118 CSNK1G1 99.10 4.10E-15 5.60E-19 139.60 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
Taok2 Tao2
Serine/threonine-protein kinase TAO2 (EC 2.7.11.1) (Thousand and one amino acid protein 2)
2.7.11.1 Rattus norvegicus
1u5r_b Q9JLS3 99.10 3.70E-15 4.60E-19 147.40 0 0 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
Map3k14 Nik
Mitogen-activated protein kinase kinase kinase 14 (EC 2.7.11.25) (NF-kappa-beta-inducing kinase) (Serine/threonine-protein kinase NIK)
2.7.11.25 Mus musculus
4g3f_a Q9WUL6 99.30 3.30E-16 4.40E-20 151.70 0 0 1 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
CDC42BPB KIAA1124
Serine/threonine-protein kinase MRCK beta (EC 2.7.11.1) (CDC42-binding protein kinase beta) (CDC42BP-beta) (DMPK-like beta) (Myotonic dystrophy kinase-related CDC42-binding kinase beta) (MRCK beta) (Myotonic dystrophy protein kinase-like beta)
2.7.11.1 Homo sapiens
Myotonic Dystrophy,Epidermolysis Bullosa Simplex, Dowling-Meara Type
5ote_a Q9Y5S2 ENSG00000198752 CDC42BPB 99.20 2.80E-15 3.60E-19 151.50 1 1 0 0 0 0 0 0
YGR188C BUB1 SGDID:S000003420
STK24 MST3 STK3
Serine/threonine-protein kinase 24 (EC 2.7.11.1) (Mammalian STE20-like protein kinase 3) (MST-3) (STE20-like kinase MST3) [Cleaved into: Serine/threonine-protein kinase 24 36 kDa subunit (Mammalian STE20-like protein kinase 3 N-terminal) (MST3/N); Serine/threonine-protein kinase 24 12 kDa subunit (Mammalian STE20-like protein kinase 3 C-terminal) (MST3/C)]
2.7.11.1 Homo sapiens
Bartter Disease,Renal Tubular Transport Disease,Pseudohypoaldosteronism,Myeloproliferative Syndrome, Transient,Arthrogryposis, Distal, Type 3,Cerebral Cavernous Malformations,Cerebrocostomandibular Syndrome,Cerebral Cavernous Malformations 3,Distal Arthrogryposis,Inflammatory Bowel Disease 14,Hypertension, Essential,Gitelman Syndrome
3a7i_a Q9Y6E0 ENSG00000102572 STK24 99.10 7.30E-15 9.50E-19 140.50 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab