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

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YCR091W KIN82 / SGDID:S000000687
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
YCR091W KIN82 SGDID:S000000687
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 99.80 5.10E-26 5.80E-30 231.10 0 0 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
GRK6 GPRK6
G protein-coupled receptor kinase 6 (EC 2.7.11.16) (G protein-coupled receptor kinase GRK6)
2.7.11.16 Homo sapiens
Whim Syndrome
3nyn_b P43250 ENSG00000198055 GRK6 99.70 1.80E-22 1.90E-26 219.00 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
GSK3B
Glycogen synthase kinase-3 beta (GSK-3 beta) (EC 2.7.11.26) (Serine/threonine-protein kinase GSK3B) (EC 2.7.11.1)
2.7.11.26 Homo sapiens
Liver Disease,Endometrial Cancer,Epilepsy,Polycystic Kidney Disease,Diabetes Mellitus,Alzheimer Disease,Major Depressive Disorder,Neuroblastoma,Cervical Non-Keratinizing Squamous Cell Carcinoma,Barbiturate Dependence,Alzheimer Disease 9,Dementia,Fallopian Tube Serous Adenocarcinoma,Breast Cancer,Parkinson Disease, Late-Onset,Colorectal Cancer,Parkinson Disease 1, Autosomal Dominant,Hepatocellular Carcinoma,Bipolar Disorder,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Type 2 Diabetes Mellitus,Schizophrenia,Ophthalmomyiasis,Familial Adenomatous Polyposis,Severe Congenital Neutropenia,Aneurysmal Bone Cysts,Attention Deficit-Hyperactivity Disorder,Medulloblastoma,Frontotemporal Dementia,Pancreatic Cancer
1j1b_b P49841 ENSG00000082701 GSK3B 99.70 9.90E-22 1.20E-25 198.30 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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
6fhb_a P53355 ENSG00000196730 DAPK1 99.70 1.40E-21 1.60E-25 191.10 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
Prkcb Pkcb Prkcb1
Protein kinase C beta type (PKC-B) (PKC-beta) (EC 2.7.11.13)
2.7.11.13 Rattus norvegicus
3pfq_a P68403 99.70 3.40E-22 3.80E-26 216.60 0 0 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 8.10E-23 9.60E-27 199.80 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.80 1.90E-25 2.20E-29 225.50 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.80 2.90E-25 3.40E-29 225.70 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 1.40E-21 1.70E-25 189.70 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.80 9.20E-24 1.10E-27 208.70 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 2.40E-22 2.80E-26 197.90 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
STK38 NDR1
Serine/threonine-protein kinase 38 (EC 2.7.11.1) (NDR1 protein kinase) (Nuclear Dbf2-related kinase 1)
2.7.11.1 Homo sapiens
Myeloproliferative Syndrome, Transient,Wilson-Turner X-Linked Mental Retardation Syndrome
6bxi_a Q15208 ENSG00000112079 STK38 99.70 1.90E-21 2.30E-25 189.70 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.80 2.90E-24 3.50E-28 209.60 0 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
PRKCI DXS1179E
Protein kinase C iota type (EC 2.7.11.13) (Atypical protein kinase C-lambda/iota) (PRKC-lambda/iota) (aPKC-lambda/iota) (nPKC-iota)
2.7.11.13 Homo sapiens
Glioblastoma,Lung Squamous Cell Carcinoma,Lung Cancer
3a8x_a P41743 ENSG00000163558 PRKCI 99.70 6.70E-23 8.00E-27 200.20 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 1.70E-21 2.00E-25 190.70 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 1.60E-21 1.90E-25 191.50 0 0 1 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
aurkb-a airk2-a
Aurora kinase B-A (EC 2.7.11.1) (Aurora/IPL1-related kinase 2-A) (AIRK2-A) (XAIRK2-A) (Serine/threonine-protein kinase 12-A) (Serine/threonine-protein kinase aurora-B-A) (xAurora-B)
2.7.11.1 Xenopus laevis
4c2v_b Q6DE08 99.70 1.30E-21 1.60E-25 183.80 0 0 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
STRADA LYK5 STRAD
STE20-related kinase adapter protein alpha (STRAD alpha) (STE20-related adapter protein) (Serologically defined breast cancer antigen NY-BR-96)
Homo sapiens
Epilepsy,Polyhydramnios,Endometrial Squamous Cell Carcinoma,Breast Cancer,Megalencephaly,Benign Epilepsy With Centrotemporal Spikes,Scheuermann Disease,Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy
2wtk_b Q7RTN6 ENSG00000266173 STRADA 99.70 5.90E-22 6.90E-26 196.90 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 6.20E-22 7.20E-26 197.70 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 4.30E-22 5.10E-26 198.20 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
STK32A YANK1
Serine/threonine-protein kinase 32A (EC 2.7.11.1) (Yet another novel kinase 1)
2.7.11.1 Homo sapiens
4fr4_a Q8WU08 ENSG00000169302 STK32A 99.70 2.50E-21 2.90E-25 194.50 0 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 2.30E-21 2.70E-25 188.20 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
MASTL GW GWL THC2
Serine/threonine-protein kinase greatwall (GW) (GWL) (hGWL) (EC 2.7.11.1) (Microtubule-associated serine/threonine-protein kinase-like) (MAST-L)
2.7.11.1 Homo sapiens
Autosomal Thrombocytopenia With Normal Platelets,Sick Building Syndrome,Thrombocytopenia,Thrombocytopenia 2,Gray Platelet Syndrome,Ceroid Lipofuscinosis, Neuronal, 2
5loh_a Q96GX5 ENSG00000120539 MASTL 99.80 4.10E-24 4.80E-28 211.30 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 2.30E-21 2.80E-25 185.40 0 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.80 4.70E-25 5.40E-29 224.00 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.80 9.20E-24 1.10E-27 207.60 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
cgd4_240
cgd4_240
Cryptosporidium parvum
3eb0_a A3FQN0 99.70 8.20E-22 9.40E-26 198.00 0 0 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
SGK1 SGK
Serine/threonine-protein kinase Sgk1 (EC 2.7.11.1) (Serum/glucocorticoid-regulated kinase 1)
2.7.11.1 Homo sapiens
Plasma Cell Neoplasm,Pseudohypoaldosteronism,Cystic Fibrosis,Gastric Cancer,Disease Of Mental Health,Liddle Syndrome 1,Body Mass Index Quantitative Trait Locus 11,Pseudohypoaldosteronism, Type I, Autosomal Dominant,Tuberous Sclerosis 1,Hypertension, Essential,Rett Syndrome,Myeloma, Multiple
2r5t_a O00141 ENSG00000118515 SGK1 99.70 2.30E-22 2.70E-26 200.40 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
PLK4 SAK STK18
Serine/threonine-protein kinase PLK4 (EC 2.7.11.21) (Polo-like kinase 4) (PLK-4) (Serine/threonine-protein kinase 18) (Serine/threonine-protein kinase Sak)
2.7.11.21 Homo sapiens
Congenital Nervous System Abnormality,Autosomal Recessive Chorioretinopathy-Microcephaly Syndrome,Colorectal Cancer,Microcephaly,Seckel Syndrome,Microcephaly And Chorioretinopathy, Autosomal Recessive, 2,Isolated Growth Hormone Deficiency,Primary Autosomal Recessive Microcephaly,Joubert Syndrome 1,Isolated Growth Hormone Deficiency, Type Ia
4jxf_a O00444 ENSG00000142731 PLK4 99.70 2.10E-21 2.70E-25 179.50 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
AURKA AIK AIRK1 ARK1 AURA AYK1 BTAK IAK1 STK15 STK6
Aurora kinase A (EC 2.7.11.1) (Aurora 2) (Aurora/IPL1-related kinase 1) (ARK-1) (Aurora-related kinase 1) (hARK1) (Breast tumor-amplified kinase) (Serine/threonine-protein kinase 15) (Serine/threonine-protein kinase 6) (Serine/threonine-protein kinase aurora-A)
2.7.11.1 Homo sapiens
Endometrial Cancer,Melanoma,Plasma Cell Neoplasm,Uterine Corpus Cancer,Atypical Teratoid Rhabdoid Tumor,Neuroblastoma,Childhood Malignant Schwannoma,Adult Malignant Schwannoma,Bladder Cancer,Laryngeal Squamous Cell Carcinoma,Tetraploidy,Ovarian Cancer,Prostate Neuroendocrine Neoplasm,Breast Cancer,Colorectal Cancer,Endometrial Serous Adenocarcinoma,Hepatocellular Carcinoma,Rhabdomyosarcoma,Gastric Cancer,Prostate Cancer,Cervical Cancer,Lynch Syndrome,Esophageal Cancer,Donohue Syndrome,Colorectal Adenocarcinoma,Myeloma, Multiple,Medulloblastoma,Primary Autosomal Recessive Microcephaly,Lung Cancer,Pancreatic Cancer
3h10_a O14965 ENSG00000087586 AURKA 99.70 2.30E-21 2.90E-25 179.90 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 2.40E-22 3.00E-26 190.40 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 7.00E-22 8.10E-26 200.80 0 0 0 0 0 0 1 0
YCR091W KIN82 SGDID:S000000687
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 99.80 7.60E-26 8.70E-30 229.30 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 6.60E-22 8.20E-26 185.90 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
OXSR1 KIAA1101 OSR1
Serine/threonine-protein kinase OSR1 (EC 2.7.11.1) (Oxidative stress-responsive 1 protein)
2.7.11.1 Homo sapiens
Bartter Disease,Arthrogryposis, Distal, Type 3,Hypomagnesemia 4, Renal,Distal Arthrogryposis,Hypomagnesemia 3, Renal
3dak_d O95747 ENSG00000172939 OXSR1 99.70 2.10E-21 2.70E-25 180.60 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
MAP4K4 HGK KIAA0687 NIK
Mitogen-activated protein kinase kinase kinase kinase 4 (EC 2.7.11.1) (HPK/GCK-like kinase HGK) (MAPK/ERK kinase kinase kinase 4) (MEK kinase kinase 4) (MEKKK 4) (Nck-interacting kinase)
2.7.11.1 Homo sapiens
Arteriovenous Malformations Of The Brain,Autosomal Recessive Distal Hereditary Motor Neuronopathy,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1,Theileriasis
4zp5_b O95819 ENSG00000071054 MAP4K4 99.70 1.60E-21 2.00E-25 184.80 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 2.70E-22 3.10E-26 199.90 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
PRKACA
cAMP-dependent protein kinase catalytic subunit alpha (PKA C-alpha) (EC 2.7.11.11)
2.7.11.11 Bos taurus
2uzv_a P00517 99.70 3.70E-23 4.40E-27 202.90 0 0 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.90 1.50E-32 1.50E-36 279.40 0 0 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
CDK1 CDC2 CDC28A CDKN1 P34CDC2
Cyclin-dependent kinase 1 (CDK1) (EC 2.7.11.22) (EC 2.7.11.23) (Cell division control protein 2 homolog) (Cell division protein kinase 1) (p34 protein kinase)
2.7.11.22,2.7.11.23, Homo sapiens
Bartholin'S Gland Adenocarcinoma,Bone Cancer,Polyploidy,Alzheimer Disease,Retinal Cancer,Neuroblastoma,Leukemia, Acute Myeloid,Hereditary Spastic Paraplegia,Leukemia, Acute Lymphoblastic,Bladder Cancer,Brain Cancer,Ovarian Cancer,Breast Cancer,Colorectal Cancer,Hepatocellular Carcinoma,Western Equine Encephalitis,Rhabdomyosarcoma,Fanconi Anemia, Complementation Group A,Neuronal Ceroid Lipofuscinosis,Breast Adenocarcinoma,Prostate Cancer,Cervical Cancer,Retinoblastoma,Lymphoma, Non-Hodgkin, Familial,Esophageal Cancer,Seckel Syndrome,Trichothiodystrophy 5, Nonphotosensitive,Mantle Cell Lymphoma,Gastrointestinal Stromal Tumor,Acute Promyelocytic Leukemia,Leukemia, Chronic Lymphocytic,Ceroid Lipofuscinosis, Neuronal, 2,Bloom Syndrome,Primary Autosomal Recessive Microcephaly,Ceroid Lipofuscinosis, Neuronal, 1,Lung Cancer,Frontotemporal Dementia
4yc3_a P06493 ENSG00000170312 CDK1 99.70 2.20E-21 2.70E-25 184.30 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 8.80E-22 1.00E-25 194.60 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 2.80E-23 3.30E-27 205.00 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 2.00E-21 2.30E-25 190.70 0 0 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 2.10E-22 2.50E-26 195.80 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.80 2.20E-24 2.70E-28 212.50 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.70 3.10E-23 3.70E-27 204.70 0 0 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
MARK3 CTAK1 EMK2
MAP/microtubule affinity-regulating kinase 3 (EC 2.7.11.1) (C-TAK1) (cTAK1) (Cdc25C-associated protein kinase 1) (ELKL motif kinase 2) (EMK-2) (Protein kinase STK10) (Ser/Thr protein kinase PAR-1) (Par-1a) (Serine/threonine-protein kinase p78)
2.7.11.1 Homo sapiens
Focal Epithelial Hyperplasia,Osteoporosis,Peutz-Jeghers Syndrome,Gaucher Disease, Type Iii,Visual Impairment And Progressive Phthisis Bulbi
3fe3_b P27448 ENSG00000075413 MARK3 99.70 1.80E-21 2.20E-25 188.50 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
GRK1 RHOK
Rhodopsin kinase GRK1 (RK) (EC 2.7.11.14) (G protein-coupled receptor kinase 1)
2.7.11.14 Bos taurus
3c4z_a P28327 99.70 9.30E-22 9.90E-26 211.20 0 0 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
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 99.80 8.40E-25 9.90E-29 215.10 1 1 0 0 0 0 0 0
YCR091W KIN82 SGDID:S000000687
GRK5 GPRK5
G protein-coupled receptor kinase 5 (EC 2.7.11.16) (G protein-coupled receptor kinase GRK5)
2.7.11.16 Homo sapiens
Systolic Heart Failure,Palmoplantar Keratoderma And Congenital Alopecia 2,Asthma
4tnd_a P34947 ENSG00000198873 GRK5 99.70 8.30E-23 8.50E-27 223.60 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab