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

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YJL187C SWE1 / SGDID:S000003723
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
YJL187C SWE1 SGDID:S000003723
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 98.90 2.70E-13 3.10E-17 134.30 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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
4qqt_a P22455 ENSG00000160867 FGFR4 98.90 1.10E-13 1.30E-17 135.10 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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
5w4w_a P48730 ENSG00000141551 CSNK1D 98.90 2.90E-13 3.40E-17 133.80 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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 98.80 3.40E-13 4.20E-17 130.70 0 0 1 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
pknE Rv1743 MTCY28.05
Serine/threonine-protein kinase PknE (EC 2.7.11.1)
2.7.11.1 Mycobacterium tuberculosis
2h34_a P9WI77 98.90 9.10E-14 1.10E-17 135.20 0 0 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
pknA Rv0015c MTCY10H4.15c
Serine/threonine-protein kinase PknA (EC 2.7.11.1)
2.7.11.1 Mycobacterium tuberculosis
6b2q_b P9WI83 98.80 4.60E-13 5.30E-17 131.60 0 0 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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
6aua_a Q06187 ENSG00000010671 BTK 98.90 2.80E-13 3.40E-17 126.20 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
MERTK MER
Tyrosine-protein kinase Mer (EC 2.7.10.1) (Proto-oncogene c-Mer) (Receptor tyrosine kinase MerTK)
2.7.10.1 Homo sapiens
Retinitis Pigmentosa,Degeneration Of Macula And Posterior Pole,Eye Degenerative Disease,Leber Plus Disease,Retinal Degeneration,Hereditary Retinal Dystrophy,Fundus Dystrophy,Retinal Disease,Achromatopsia,Usher Syndrome, Type Iiia,Choroid Disease,Stargardt Disease,Macular Degeneration, Age-Related, 1,Cone-Rod Dystrophy 2,Retinitis,Retinitis Pigmentosa 38,La Crosse Encephalitis,Usher Syndrome,Vitelliform Macular Dystrophy,Cone Dystrophy,Choroideremia,Leber Congenital Amaurosis 1,Leber Congenital Amaurosis 2,Systemic Lupus Erythematosus,Retinoschisis 1, X-Linked, Juvenile
3brb_b Q12866 ENSG00000153208 MERTK 99.00 1.90E-14 2.30E-18 139.20 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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 98.90 3.40E-13 3.90E-17 133.80 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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 98.90 1.50E-13 1.80E-17 137.00 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
TGRH88_017420
TGRH88_017420
Toxoplasma gondii
3dxn_a Q3HNM6 98.80 4.50E-13 5.30E-17 129.10 0 0 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
Pto
Pto
Solanum pimpinellifolium
2qkw_b Q40234 98.90 1.50E-13 1.80E-17 134.00 0 0 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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 99.00 4.80E-14 5.50E-18 142.60 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
pck spr1147
pck spr1147
Streptococcus pneumoniae
4r78_a Q8DPI4 98.90 9.20E-14 1.10E-17 134.80 0 0 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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 2.00E-15 2.40E-19 146.50 0 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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 98.90 1.30E-13 1.60E-17 136.60 0 0 1 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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 99.00 4.00E-14 4.70E-18 136.50 0 0 0 0 0 0 1 0
YJL187C SWE1 SGDID:S000003723
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 98.90 1.00E-13 1.20E-17 139.70 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
BN1205_040370 TGVEG_207820
BN1205_040370 TGVEG_207820
2.7.11.24 Toxoplasma gondii
3rp9_a B6KP12 98.90 3.30E-13 3.90E-17 139.30 0 0 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
Prag1 Pragmin
Inactive tyrosine-protein kinase PRAG1 (PEAK1-related kinase-activating pseudokinase 1) (Pragma of Rnd2)
Rattus norvegicus
6ewx_a D3ZMK9 99.00 5.80E-14 6.30E-18 149.60 0 0 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
DCLK1 DCAMKL1 DCDC3A KIAA0369
Serine/threonine-protein kinase DCLK1 (EC 2.7.11.1) (Doublecortin domain-containing protein 3A) (Doublecortin-like and CAM kinase-like 1) (Doublecortin-like kinase 1)
2.7.11.1 Homo sapiens
Zellweger Syndrome,Colorectal Cancer,Attention Deficit-Hyperactivity Disorder,Chemical Colitis,Band Heterotopia
5jzj_b O15075 ENSG00000133083 DCLK1 98.80 3.70E-13 4.40E-17 129.70 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
MAPK13 PRKM13 SAPK4
Mitogen-activated protein kinase 13 (MAP kinase 13) (MAPK 13) (EC 2.7.11.24) (Mitogen-activated protein kinase p38 delta) (MAP kinase p38 delta) (Stress-activated protein kinase 4)
2.7.11.24 Homo sapiens
4yno_a O15264 ENSG00000156711 MAPK13 98.90 3.20E-13 3.60E-17 137.50 0 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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 98.90 2.00E-13 2.40E-17 130.50 0 0 0 0 0 0 1 0
YJL187C SWE1 SGDID:S000003723
BIK1 At2g39660 F12L6.32 F17A14.3
Serine/threonine-protein kinase BIK1 (EC 2.7.11.1) (Protein BOTRYTIS-INDUCED KINASE 1)
2.7.11.1 Arabidopsis thaliana
5tos_a O48814 98.90 2.30E-13 2.60E-17 138.20 0 0 0 0 0 0 1 0
YJL187C SWE1 SGDID:S000003723
PBL2 APK2A KIN1 At1g14370 F14L17.14
Probable serine/threonine-protein kinase PBL2 (EC 2.7.11.1) (PBS1-like protein 2) (Protein kinase 2A)
2.7.11.1 Arabidopsis thaliana
6j5t_d O49839 98.80 3.50E-13 4.00E-17 138.50 0 0 0 0 0 0 1 0
YJL187C SWE1 SGDID:S000003723
STK17B DRAK2
Serine/threonine-protein kinase 17B (EC 2.7.11.1) (DAP kinase-related apoptosis-inducing protein kinase 2)
2.7.11.1 Homo sapiens
Colon Squamous Cell Carcinoma
3lm5_a O94768 ENSG00000081320 STK17B 98.90 1.30E-13 1.50E-17 136.60 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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 99.50 6.40E-19 6.50E-23 181.30 0 0 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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
5hu9_a P00519 ENSG00000097007 ABL1 98.90 3.20E-13 3.90E-17 127.40 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
PIM1
Serine/threonine-protein kinase pim-1 (EC 2.7.11.1)
2.7.11.1 Homo sapiens
Retinitis Pigmentosa,Polyploidy,Plasma Protein Metabolism Disease,Primary Central Nervous System Lymphoma,Diamond-Blackfan Anemia,Myeloid Leukemia,Prostate Cancer,Mantle Cell Lymphoma
3a99_a P11309 ENSG00000137193 PIM1 99.00 2.80E-14 3.20E-18 140.70 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
FGFR1 BFGFR CEK FGFBR FLG FLT2 HBGFR
Fibroblast growth factor receptor 1 (FGFR-1) (EC 2.7.10.1) (Basic fibroblast growth factor receptor 1) (BFGFR) (bFGF-R-1) (Fms-like tyrosine kinase 2) (FLT-2) (N-sam) (Proto-oncogene c-Fgr) (CD antigen CD331)
2.7.10.1 Homo sapiens
Adult Hepatocellular Carcinoma,Pancreatic Adenocarcinoma,Bone Disease,Bone Development Disease,Achondroplasia,Heart Disease,Fibrous Dysplasia,Endometrial Cancer,Apert Syndrome,Saethre-Chotzen Syndrome,Charge Syndrome,Pfeiffer Syndrome,Lymphoblastic Lymphoma,Myeloid And Lymphoid Neoplasms With Eosinophilia And Abnormalities Of Pdgfra, Pdgfrb, And Fgfr1,Retinitis Pigmentosa,Myeloid And Lymphoid Neoplasms Associated With Pdgfra Rearrangement,Myeloid And Lymphoid Neoplasms Associated With Fgfr1 Abnormalities,Brain Stem Glioma,Ossifying Fibroma,Melanoma,Chronic Eosinophilic Leukemia,Leukemia, Chronic Myeloid,Cleft Lip,Microform Holoprosencephaly,Hypogonadism,Dysostosis,B-Lymphoblastic Leukemia/Lymphoma,Neuroma,Synostosis,Rasopathy,Deafness, Autosomal Recessive 71,Congenital Hypogonadotropic Hypogonadism,Large Cell Carcinoma,Lung Large Cell Carcinoma,Holoprosencephaly,Osteochondroma,Cleft Lip/Palate,Nail Disorder, Nonsyndromic Congenital, 1,Myeloproliferative Neoplasm,Split Hand-Foot Malformation,Hypogonadotropic Hypogonadism,Semilobar Holoprosencephaly,Ankylosis,Radioulnar Synostosis,Cataract 30,Plagiocephaly,Lobar Holoprosencephaly,Leukemia,Syndromic Craniosynostosis,Craniosynostosis,Neuroblastoma,Mixed Phenotype Acute Leukemia,Pilomyxoid Astrocytoma,Pilocytic Astrocytoma,Cryptorchidism, Unilateral Or Bilateral,Hypereosinophilic Syndrome,Nevus, Epidermal,Acute Leukemia,Normosmic Congenital Hypogonadotropic Hypogonadism,Encephalocraniocutaneous Lipomatosis,Schimmelpenning-Feuerstein-Mims Syndrome,Glioma,Leukemia, Acute Myeloid,Phosphorus Metabolism Disease,Hematologic Cancer,Fibrolamellar Carcinoma,Leukemia, Acute Lymphoblastic,Hepatocellular Clear Cell Carcinoma,Chondroblastoma,Rosette-Forming Glioneuronal Tumor,Dysembryoplastic Neuroepithelial Tumor,Fgfr Craniosynostosis Syndromes,Sensorineural Hearing Loss,Choanal Atresia, Posterior,Infertility,Bladder Cancer,Primary Hypereosinophilic Syndrome,Megaesophagus,Osteoglophonic Dysplasia,Synovial Chondromatosis,Adenocarcinoma,Breast Carcinoma In Situ,Breast Cancer,Glioblastoma,Gliosarcoma,Giant Cell Glioblastoma,Colorectal Cancer,Isolated Trigonocephaly,Hepatocellular Carcinoma,8p11 Myeloproliferative Syndrome,Lipomatosis,Oligodendroglioma,Childhood Oligodendroglioma,Spinal Cord Oligodendroglioma,Adult Oligodendroglioma,Rhabdomyosarcoma,Hartsfield Syndrome,Muenke Syndrome,Pseudopterygium,Chromosome 8p11 Myeloproliferative Syndrome,Spotted Fever,Sarcoma,Cleft Palate, Isolated,Cleidocranial Dysplasia,Coloboma Of Macula,Gastric Cancer,Systemic Mastocytosis,Prostate Cancer,Disease Of Mental Health,Mastocytosis,Jackson-Weiss Syndrome,Body Mass Index Quantitative Trait Locus 11,Kallmann Syndrome,Crouzon Syndrome,Gastric Adenocarcinoma,Lung Squamous Cell Carcinoma,Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1,Bladder Urothelial Carcinoma,Holoprosencephaly 1,Septooptic Dysplasia,Hypophosphatemia,Antley-Bixler Syndrome,Esophageal Cancer,Hypertelorism, Microtia, Facial Clefting Syndrome,Odontochondrodysplasia,Orofacial Cleft,Chromosome 2q35 Duplication Syndrome,Tooth Agenesis,Thanatophoric Dysplasia, Type I,Trigonocephaly 1,Renal Hypodysplasia/Aplasia 1,Lymphoblastic Leukemia, Acute, With Lymphomatous Features,Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans,Salivary Gland Carcinoma,Hypochondroplasia,Hypogonadotropic Hypogonadism 7 With Or Without Anosmia,Lymphoma,Hypophosphatemic Rickets, X-Linked Dominant,Hypogonadotropic Hypogonadism 1 With Or Without Anosmia,Hypogonadotropic Hypogonadism 2 With Or Without Anosmia,Lacrimoauriculodentodigital Syndrome,Myelofibrosis,Medulloblastoma,Atypical Chronic Myeloid Leukemia,Neuroblastoma 1,C Syndrome,Tumoral Calcinosis, Hyperphosphatemic, Familial, 1,Lung Cancer,Oculoectodermal Syndrome,Cerebellar Hypoplasia/Atrophy, Epilepsy, And Global Developmental Delay,Pancreatic Cancer
3tt0_a P11362 ENSG00000077782 FGFR1 98.80 4.60E-13 5.20E-17 136.00 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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
5ita_b P15056 ENSG00000157764 BRAF 99.00 3.40E-14 4.00E-18 137.50 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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 98.90 1.80E-13 2.10E-17 136.90 1 1 0 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
Rps6ka3 Mapkapk1b Rps6ka-rs1 Rsk2
Ribosomal protein S6 kinase alpha-3 (S6K-alpha-3) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 3) (p90-RSK 3) (p90RSK3) (MAP kinase-activated protein kinase 1b) (MAPK-activated protein kinase 1b) (MAPKAP kinase 1b) (MAPKAPK-1b) (Ribosomal S6 kinase 2) (RSK-2) (pp90RSK2)
2.7.11.1 Mus musculus
5o1s_a P18654 98.90 2.50E-13 2.80E-17 137.70 0 0 1 0 0 0 0 0
YJL187C SWE1 SGDID:S000003723
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 99.00 7.00E-14 8.70E-18 130.90 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab