YGL119W COQ8 / SGDID:S000003087
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
YGL119W COQ8 SGDID:S000003087
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 1.80E-23 1.40E-27 203.50 0 0 0 0 0 0 0 0
YGL119W COQ8 SGDID:S000003087
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 1.80E-21 1.40E-25 193.30 1 1 0 0 0 0 0 0
YGL119W COQ8 SGDID:S000003087
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 8.90E-16 6.80E-20 150.90 1 1 0 0 0 0 0 0
YGL119W COQ8 SGDID:S000003087
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 5.60E-16 4.30E-20 153.20 1 1 0 0 0 0 0 0
YGL119W COQ8 SGDID:S000003087
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 7.30E-16 5.60E-20 152.90 1 1 0 0 0 0 0 0
YGL119W COQ8 SGDID:S000003087
Rv3197
Rv3197
 Mycobacterium tuberculosis
5yk0_a O53343 100.00 3.60E-49 2.70E-53 409.10 0 0 0 0 0 0 0 0
YGL119W COQ8 SGDID:S000003087
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 9.20E-16 7.10E-20 155.60 0 0 1 0 0 0 0 0
YGL119W COQ8 SGDID:S000003087
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 8.50E-16 6.50E-20 153.60 0 0 0 0 0 0 1 0
YGL119W COQ8 SGDID:S000003087
GRK2 ADRBK1 BARK BARK1
Beta-adrenergic receptor kinase 1 (Beta-ARK-1) (EC 2.7.11.15) (G-protein coupled receptor kinase 2)
 2.7.11.15 Homo sapiens
Heart Disease,Alzheimer Disease,Myocardial Infarction,Exudative Vitreoretinopathy 5,Colorectal Cancer,Disease Of Mental Health,Hypertension, Essential
 3v5w_a P25098 ENSG00000173020 GRK2 99.50 8.50E-19 6.20E-23 187.50 1 1 0 0 0 0 0 0
YGL119W COQ8 SGDID:S000003087
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 99.20 9.80E-16 7.50E-20 149.20 0 0 1 0 0 0 0 0
YGL119W COQ8 SGDID:S000003087
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 99.40 5.50E-17 4.20E-21 164.20 1 1 0 0 0 0 0 0
YGL119W COQ8 SGDID:S000003087
COQ8A ADCK3 CABC1 PP265
Atypical kinase COQ8A, mitochondrial (EC 2.7.-.-) (Chaperone activity of bc1 complex-like) (Chaperone-ABC1-like) (Coenzyme Q protein 8A) (aarF domain-containing protein kinase 3)
 2.7.-.- Homo sapiens
Mitochondrial Encephalomyopathy,Nephrotic Syndrome,Pathologic Nystagmus,Chronic Progressive External Ophthalmoplegia,Leigh Syndrome With Nephrotic Syndrome,Cerebellar Disease,Mitochondrial Disorders,Spinocerebellar Ataxia, Autosomal Recessive 14,Cardiofaciocutaneous Syndrome 1,Multiple Acyl-Coa Dehydrogenase Deficiency,Aceruloplasminemia,Mental Retardation, X-Linked, With Cerebellar Hypoplasia And Distinctive Facial Appearance,Spinocerebellar Ataxia, Autosomal Recessive 8,Coenzyme Q10 Deficiency, Primary, 4,Coenzyme Q10 Deficiency, Primary, 7,Coenzyme Q10 Deficiency Disease,Marinesco-Sjogren Syndrome,Autosomal Recessive Cerebellar Ataxia,Hereditary Ataxia,Spastic Ataxia,Joubert Syndrome 17,Coenzyme Q10 Deficiency, Primary, 6,Coenzyme Q10 Deficiency, Primary, 5,Spastic Paraplegia 7, Autosomal Recessive,Coenzyme Q10 Deficiency, Primary, 1,Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis,Mitochondrial Complex I Deficiency, Nuclear Type 1,Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia,Kearns-Sayre Syndrome,Leigh Syndrome
 4ped_a Q8NI60 ENSG00000163050 COQ8A 100.00 1.60E-48 1.20E-52 396.60 1 1 0 0 0 0 0 0
YGL119W COQ8 SGDID:S000003087
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 99.60 2.20E-19 1.70E-23 178.40 1 1 0 0 0 0 0 0
YGL119W COQ8 SGDID:S000003087
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 8.80E-16 6.80E-20 150.40 1 1 0 0 0 0 0 0
YGL119W COQ8 SGDID:S000003087
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 6.10E-16 4.60E-20 156.40 0 0 0 0 0 0 1 0
YGL119W COQ8 SGDID:S000003087
EPHA3 ETK ETK1 HEK TYRO4
Ephrin type-A receptor 3 (EC 2.7.10.1) (EPH-like kinase 4) (EK4) (hEK4) (HEK) (Human embryo kinase) (Tyrosine-protein kinase TYRO4) (Tyrosine-protein kinase receptor ETK1) (Eph-like tyrosine kinase 1)
 2.7.10.1 Homo sapiens
Large Cell Carcinoma,Lung Large Cell Carcinoma,Cerebral Artery Occlusion,Adenocarcinoma,Breast Cancer,Beriberi,Parkinson Disease, Late-Onset,Colorectal Cancer,Thiamine Deficiency Disease,Tumoral Calcinosis, Hyperphosphatemic, Familial, 1,Wet Beriberi
 2qol_a P29320 ENSG00000044524 EPHA3 99.30 2.10E-16 1.60E-20 156.90 1 1 0 0 0 0 0 0