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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YPL239W | YAR1 | SGDID:S000006160 | NAS6 YGR232W G8564 |
Probable 26S proteasome regulatory subunit p28 (Proteasome non-ATPase subunit 6) |
Saccharomyces cerevisiae | 1wg0_a | P50086 | 98.20 | 4.20E-10 | 4.20E-14 | 83.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | ASB11 |
Ankyrin repeat and SOCS box protein 11 (ASB-11) |
Homo sapiens | Lacrimal Duct Obstruction |
4uuc_a | Q8WXH4 | ENSG00000165192 | ASB11 | 98.20 | 3.90E-10 | 3.90E-14 | 82.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL239W | YAR1 | SGDID:S000006160 | Kank1 |
Kank1 |
Mus musculus | 5yay_a | E9Q238 | 98.30 | 2.20E-10 | 2.10E-14 | 88.20 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | legAS4 lpg1718 |
legAS4 lpg1718 |
Legionella pneumophila | 5czy_a | Q5ZUS4 | 98.00 | 2.10E-09 | 1.90E-13 | 93.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | EHMT1 EUHMTASE1 GLP KIAA1876 KMT1D |
Histone-lysine N-methyltransferase EHMT1 (EC 2.1.1.-) (Euchromatic histone-lysine N-methyltransferase 1) (Eu-HMTase1) (G9a-like protein 1) (GLP) (GLP1) (Histone H3-K9 methyltransferase 5) (H3-K9-HMTase 5) (Lysine N-methyltransferase 1D) |
2.1.1.- | Homo sapiens | Kleefstra Syndrome,Deafness, Autosomal Dominant 47,Hypoplastic Left Heart Syndrome,Polymicrogyria,Kleefstra Syndrome Due To A Point Mutation,Pontocerebellar Hypoplasia, Type 2a,Weaver Syndrome,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Kleefstra Syndrome 1,Chromosome 16p13.3 Deletion Syndrome, Proximal,Pitt-Hopkins Syndrome,Schizophrenia,Ogden Syndrome,Autism Spectrum Disorder,Kabuki Syndrome 1,Autosomal Dominant Non-Syndromic Intellectual Disability,Chromosomal Deletion Syndrome,Autism,Christianson Syndrome |
3b7b_a | Q9H9B1 | ENSG00000181090 | EHMT1 | 98.30 | 1.90E-10 | 1.90E-14 | 85.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL239W | YAR1 | SGDID:S000006160 | NOTCH1 TAN1 |
Neurogenic locus notch homolog protein 1 (Notch 1) (hN1) (Translocation-associated notch protein TAN-1) [Cleaved into: Notch 1 extracellular truncation (NEXT); Notch 1 intracellular domain (NICD)] |
Homo sapiens | Ventricular Septal Defect,Heart Septal Defect,Heart Disease,Richter'S Syndrome,Squamous Cell Carcinoma,Severe Combined Immunodeficiency,Lymphoblastic Lymphoma,Retinitis Pigmentosa,Myeloid And Lymphoid Neoplasms Associated With Fgfr1 Abnormalities,Ossifying Fibroma,Adenoid Cystic Carcinoma,Double Outlet Right Ventricle,Hajdu-Cheney Syndrome,Bone Cancer,Atrial Heart Septal Defect,Invasive Bladder Transitional Cell Carcinoma,Prion Disease,Connective Tissue Disease,Uterine Adnexa Cancer,Kleefstra Syndrome,Tongue Carcinoma,Orofacial Cleft 4,Clear Cell Renal Cell Carcinoma,Aortic Dissection,Alzheimer Disease,Rasopathy,Nodular Regenerative Hyperplasia,Mucoepidermoid Carcinoma,T-Cell Non-Hodgkin Lymphoma,Holoprosencephaly,Plasmablastic Lymphoma,T-Cell Lymphoblastic Leukemia/Lymphoma,Biliary Tract Disease,Infratentorial Cancer,Familial Thoracic Aortic Aneurysm And Aortic Dissection,Leukemia,Colon Adenocarcinoma,Neuroblastoma,Hypoplastic Left Heart Syndrome,Lacrimal Gland Adenoid Cystic Carcinoma,Shone Complex,Acute Leukemia,Intrahepatic Cholangiocarcinoma,Leukemia, Acute Myeloid,Bone Marrow Cancer,Basal Cell Carcinoma,Hematologic Cancer,Hemangioma,Leukemia, Acute Lymphoblastic,Combined Immunodeficiency,Basal Cell Nevus Syndrome,Aortic Disease,Aortic Valve Disease 1,Focal Segmental Glomerulosclerosis,Brain Cancer,Precursor T-Cell Acute Lymphoblastic Leukemia,Lung Adenoma,Oropharynx Cancer,Aplastic Anemia,Ovarian Cancer,T-Cell Acute Lymphoblastic Leukemia,Breast Cancer,Tonsil Cancer,Exudative Vitreoretinopathy 5,Microphthalmia,Malignant Astrocytoma,Adult Liposarcoma,Breast Liposarcoma,Anaplastic Astrocytoma,Colorectal Cancer,Peripheral Nervous System Disease,Hepatocellular Carcinoma,Splenic Diffuse Red Pulp Small B-Cell Lymphoma,Pheochromocytoma,Aneurysm,Hydrocephalus,Tongue Disease,Cerebral Degeneration,Spondylocostal Dysostosis 3, Autosomal Recessive,Alagille Syndrome 1,Skin Carcinoma,Hemophagocytic Lymphohistiocytosis, Familial, 2,Gastric Cancer,Friedreich Ataxia,Prostate Cancer,Disease Of Mental Health,Cervical Cancer,Aortic Aneurysm,Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, Type 1,Orofacial Cleft 8,Scalp-Ear-Nipple Syndrome,Lung Squamous Cell Carcinoma,Adenoiditis,Merkel Cell Carcinoma,Lymphoma, Non-Hodgkin, Familial,Mouth Disease,Adams-Oliver Syndrome 5,Loeys-Dietz Syndrome,Hypoplastic Left Heart Syndrome 1,Tetralogy Of Fallot,Myelodysplastic Syndrome,Mantle Cell Lymphoma,Peripheral T-Cell Lymphoma,Heart, Malformation Of,Tongue Squamous Cell Carcinoma,Acute Promyelocytic Leukemia,Bone Squamous Cell Carcinoma,Aortic Aneurysm, Familial Thoracic 1,Endosteal Hyperostosis, Autosomal Dominant,Wilms Tumor 1,Mental Retardation, Autosomal Dominant 40,Lipoprotein Quantitative Trait Locus,Cardiovascular Organ Benign Neoplasm,Brain Glioma,Patent Ductus Arteriosus 1,Adams-Oliver Syndrome,Wilson-Turner X-Linked Mental Retardation Syndrome,Dowling-Degos Disease,Leukemia, Chronic Lymphocytic,Marfan Syndrome,Left Ventricular Noncompaction,Myeloma, Multiple,Medulloblastoma,Lung Cancer,Oliver Syndrome,Pancreatic Cancer |
2f8y_a | P46531 | ENSG00000148400 | NOTCH1 | 98.20 | 4.60E-10 | 4.60E-14 | 81.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL239W | YAR1 | SGDID:S000006160 | ZDHHC17 HIP14 HIP3 HYPH KIAA0946 HSPC294 |
Palmitoyltransferase ZDHHC17 (EC 2.3.1.225) (Acyltransferase ZDHHC17) (EC 2.3.1.-) (DHHC domain-containing cysteine-rich protein 17) (DHHC17) (Huntingtin yeast partner H) (Huntingtin-interacting protein 14) (HIP-14) (Huntingtin-interacting protein 3) (HIP-3) (Huntingtin-interacting protein H) (Putative MAPK-activating protein PM11) (Putative NF-kappa-B-activating protein 205) (Zinc finger DHHC domain-containing protein 17) |
2.3.1.225 | Homo sapiens | Huntington Disease,Hypoparathyroidism, X-Linked |
3eu9_a | Q8IUH5 | ENSG00000186908 | ZDHHC17 | 98.40 | 5.80E-11 | 5.70E-15 | 88.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL239W | YAR1 | SGDID:S000006160 | Lebu_0176 |
Lebu_0176 |
Leptotrichia buccalis | 3t8k_a | C7NDE2 | 98.10 | 1.20E-09 | 1.20E-13 | 78.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | KANK1 ANKRD15 KANK KIAA0172 |
KN motif and ankyrin repeat domain-containing protein 1 (Ankyrin repeat domain-containing protein 15) (Kidney ankyrin repeat-containing protein) |
Homo sapiens | Metanephric Adenoma,Chromosome 9p Deletion Syndrome,Nephrotic Syndrome,Cerebral Palsy,Inherited Congenital Spastic Tetraplegia,Cerebral Palsy, Spastic Quadriplegic, 2,Myeloproliferative Neoplasm,Quadriplegia,Renal Adenoma,Tukel Syndrome,Spastic Quadriplegia,Spastic Cerebral Palsy,Brain Glioma,Autosomal Dominant Non-Syndromic Intellectual Disability |
5ybu_a | Q14678 | ENSG00000107104 | KANK1 | 98.30 | 1.80E-10 | 1.80E-14 | 87.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL239W | YAR1 | SGDID:S000006160 | Espn |
Espin (Ectoplasmic specialization protein) |
Mus musculus | 5et1_b | Q9ET47 | 98.20 | 3.00E-10 | 2.90E-14 | 90.00 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | spa |
Immunoglobulin G-binding protein A (IgG-binding protein A) (Staphylococcal protein A) (SpA) |
Staphylococcus aureus | 5cbn_a | P38507 | 98.40 | 1.10E-10 | 1.00E-14 | 85.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | Tnks Tnks1 |
Poly [ADP-ribose] polymerase tankyrase-1 (EC 2.4.2.30) (ADP-ribosyltransferase diphtheria toxin-like 5) (ARTD5) (Protein poly-ADP-ribosyltransferase tankyrase-1) (EC 2.4.2.-) (TRF1-interacting ankyrin-related ADP-ribose polymerase 1) (Tankyrase I) (Tankyrase-1) (TANK1) |
2.4.2.30 | Mus musculus | 6cf6_a | Q6PFX9 | 98.40 | 9.30E-11 | 9.30E-15 | 92.10 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YPL239W | YAR1 | SGDID:S000006160 | NFKBIA IKBA MAD3 NFKBI |
NF-kappa-B inhibitor alpha (I-kappa-B-alpha) (IkB-alpha) (IkappaBalpha) (Major histocompatibility complex enhancer-binding protein MAD3) |
Homo sapiens | Vascular Disease,Stomach Carcinoma In Situ,Bone Cancer,Leukemia, Chronic Myeloid,Diabetes Mellitus,Hepatitis B,Mycobacterium Malmoense,Ectodermal Dysplasia,B-Cell Lymphoma,Osteomyelitis, Sterile Multifocal, With Periostitis And Pustulosis,T-Cell Lymphoblastic Leukemia/Lymphoma,Carbuncle,Shigellosis,Periostitis,Hypohidrotic Ectodermal Dysplasia With Immunodeficiency,Newcastle Disease,Legionellosis,Ovarian Cancer,Burkitt Lymphoma,T-Cell Acute Lymphoblastic Leukemia,Crohn'S Disease,Squamous Cell Carcinoma, Head And Neck,Malignant Astrocytoma,Gliosarcoma,Giant Cell Glioblastoma,Parkinson Disease, Late-Onset,Colorectal Cancer,Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive,Hepatocellular Carcinoma,Human Immunodeficiency Virus Type 1,Tropical Spastic Paraparesis,Chromosome 14q11-Q22 Deletion Syndrome,Cardiomyopathy, Dilated, 1gg,Breast Adenocarcinoma,Cone-Rod Dystrophy 2,Prostate Cancer,Disease Of Mental Health,Rheumatoid Arthritis,Adult T-Cell Leukemia,Inflammatory Bowel Disease,Immune Deficiency Disease,Myelodysplastic Syndrome,Intellectual Developmental Disorder, X-Linked 108,Ectodermal Dysplasia And Immunodeficiency 2,Mantle Cell Lymphoma,Nasopharyngeal Carcinoma,Psoriatic Arthritis,Leukemia, Chronic Lymphocytic,Systemic Lupus Erythematosus,Myeloma, Multiple,Lung Cancer,Helicobacter Pylori Infection,Asthma,Pancreatic Cancer |
1ikn_d | P25963 | 98.50 | 1.90E-11 | 1.70E-15 | 95.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YPL239W | YAR1 | SGDID:S000006160 | Notch1 Motch |
Neurogenic locus notch homolog protein 1 (Notch 1) (Motch A) (mT14) (p300) [Cleaved into: Notch 1 extracellular truncation (NEXT); Notch 1 intracellular domain (NICD)] |
Mus musculus | 1ymp_a | Q01705 | 98.40 | 1.00E-10 | 1.00E-14 | 78.90 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | ANKRD27 PP12899 |
Ankyrin repeat domain-containing protein 27 (VPS9 domain-containing protein) |
Homo sapiens | Parastremmatic Dwarfism,Hermansky-Pudlak Syndrome,Pontiac Fever |
4b93_b | Q96NW4 | ENSG00000105186 | ANKRD27 | 98.20 | 2.90E-10 | 2.80E-14 | 88.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL239W | YAR1 | SGDID:S000006160 | TNKS PARP5A PARPL TIN1 TINF1 TNKS1 |
Poly [ADP-ribose] polymerase tankyrase-1 (EC 2.4.2.30) (ADP-ribosyltransferase diphtheria toxin-like 5) (ARTD5) (Poly [ADP-ribose] polymerase 5A) (Protein poly-ADP-ribosyltransferase tankyrase-1) (EC 2.4.2.-) (TNKS-1) (TRF1-interacting ankyrin-related ADP-ribose polymerase) (Tankyrase I) (Tankyrase-1) (TANK1) |
2.4.2.30 | Homo sapiens | Cornelia De Lange Syndrome,Lung Acinar Adenocarcinoma,Amyotrophic Lateral Sclerosis 1,Arthrogryposis, Renal Dysfunction, And Cholestasis 2,Cherubism,Meningioma, Familial,Arthrogryposis, Renal Dysfunction, And Cholestasis 1 |
5jhq_d | O95271 | ENSG00000173273 | TNKS | 98.10 | 9.70E-10 | 9.60E-14 | 90.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL239W | YAR1 | SGDID:S000006160 | K1L |
K1L |
Vaccinia virus | 3kea_b | Q6IV60 | 98.00 | 1.80E-09 | 1.70E-13 | 82.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | AKR2A AFT AKR2 At4g35450 F15J1.20 |
Ankyrin repeat domain-containing protein 2A (AtAKR2) |
Arabidopsis thaliana | 4tum_c | Q9SAR5 | 98.00 | 1.70E-09 | 1.70E-13 | 71.80 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | Cdkn2b |
Cyclin-dependent kinase 4 inhibitor B (p14-INK4b) (p15-INK4b) |
Mus musculus | 1d9s_a | P55271 | 98.00 | 1.70E-09 | 1.70E-13 | 71.70 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | Trpv6 |
Transient receptor potential cation channel subfamily V member 6 (TrpV6) (Calcium transport protein 1) (CaT1) (Epithelial calcium channel 2) (ECaC2) |
Mus musculus | 2rfa_a | Q91WD2 | 98.10 | 1.40E-09 | 1.40E-13 | 80.20 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | RFXANK ANKRA1 RFXB |
DNA-binding protein RFXANK (Ankyrin repeat family A protein 1) (Regulatory factor X subunit B) (RFX-B) (Regulatory factor X-associated ankyrin-containing protein) |
Homo sapiens | Severe Combined Immunodeficiency,Tibial Neuropathy,Tarsal Tunnel Syndrome,Combined Immunodeficiency,Discharging Ear,Purine Nucleoside Phosphorylase Deficiency,Alcoholic Gastritis,Acquired Thrombocytopenia,Omenn Syndrome,Retinitis Pigmentosa 48,Bare Lymphocyte Syndrome, Type I,Immune Deficiency Disease,Bare Lymphocyte Syndrome, Type Ii,Tumoral Calcinosis, Hyperphosphatemic, Familial, 1,Bjornstad Syndrome |
3uxg_a | O14593 | ENSG00000064490 | RFXANK | 98.10 | 7.40E-10 | 7.40E-14 | 77.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL239W | YAR1 | SGDID:S000006160 | Nfkbib Ikbb |
NF-kappa-B inhibitor beta (NF-kappa-BIB) (I-kappa-B-beta) (IkB-B) (IkB-beta) (IkappaBbeta) |
Mus musculus | 1k3z_d | Q60778 | 98.40 | 5.40E-11 | 5.30E-15 | 90.70 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | ANKRA2 ANKRA |
Ankyrin repeat family A protein 2 (RFXANK-like protein 2) |
Homo sapiens | Donnai-Barrow Syndrome,Three M Syndrome 1,Branchiooculofacial Syndrome |
3so8_a | Q9H9E1 | ENSG00000164331 | ANKRA2 | 98.50 | 1.60E-11 | 1.50E-15 | 87.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL239W | YAR1 | SGDID:S000006160 | YAR1 YPL239W |
Ankyrin repeat-containing protein YAR1 |
Saccharomyces cerevisiae | 4bsz_b | P46683 | 99.10 | 8.50E-15 | 8.40E-19 | 107.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | PPP1R13L IASPP NKIP1 PPP1R13BL RAI |
RelA-associated inhibitor (Inhibitor of ASPP protein) (Protein iASPP) (NFkB-interacting protein 1) (PPP1R13B-like protein) |
Homo sapiens | Basal Cell Carcinoma,Dilated Cardiomyopathy,Noonan Syndrome With Multiple Lentigines |
2vge_a | Q8WUF5 | ENSG00000104881 | PPP1R13L | 98.20 | 4.40E-10 | 4.30E-14 | 84.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL239W | YAR1 | SGDID:S000006160 | LMJF_29_1100 |
LMJF_29_1100 |
Leishmania major | 3ljn_a | E9ADW8 | 98.20 | 3.20E-10 | 3.20E-14 | 89.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | ACAP2 CENTB2 KIAA0041 |
Arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2 (Centaurin-beta-2) (Cnt-b2) |
Homo sapiens | Tethered Spinal Cord Syndrome |
6if3_a | Q15057 | ENSG00000114331 | ACAP2 | 98.20 | 2.90E-10 | 2.70E-14 | 83.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL239W | YAR1 | SGDID:S000006160 | TNKS2 PARP5B TANK2 TNKL |
Poly [ADP-ribose] polymerase tankyrase-2 (EC 2.4.2.30) (ADP-ribosyltransferase diphtheria toxin-like 6) (ARTD6) (Poly [ADP-ribose] polymerase 5B) (Protein poly-ADP-ribosyltransferase tankyrase-2) (EC 2.4.2.-) (TNKS-2) (TRF1-interacting ankyrin-related ADP-ribose polymerase 2) (Tankyrase II) (Tankyrase-2) (TANK2) (Tankyrase-like protein) (Tankyrase-related protein) |
2.4.2.30 | Homo sapiens | Familial Isolated Hypoparathyroidism,Arthrogryposis, Renal Dysfunction, And Cholestasis 2,Cherubism,Arthrogryposis, Renal Dysfunction, And Cholestasis 1 |
5bxo_a | Q9H2K2 | ENSG00000107854 | TNKS2 | 98.00 | 1.50E-09 | 1.50E-13 | 76.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL239W | YAR1 | SGDID:S000006160 | CDKN2C CDKN6 |
Cyclin-dependent kinase 4 inhibitor C (Cyclin-dependent kinase 6 inhibitor) (p18-INK4c) (p18-INK6) |
Homo sapiens | Plasma Cell Neoplasm,Retinal Cancer,Parathyroid Adenoma,Leukemia, Acute Lymphoblastic,Ovarian Cancer,Breast Cancer,Multiple Endocrine Neoplasia,Oligodendroglioma,Pheochromocytoma,Retinoblastoma,Chromophobe Adenoma,Multiple Endocrine Neoplasia, Type Iv,Lymphoma, Non-Hodgkin, Familial,Multiple Endocrine Neoplasia, Type I,Meningioma, Familial,Lymphoma,Myeloma, Multiple,Medulloblastoma,Melanoma, Cutaneous Malignant 1,Lung Cancer |
1bu9_a | P42773 | 98.00 | 1.90E-09 | 1.90E-13 | 74.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YPL239W | YAR1 | SGDID:S000006160 | EF_0377 |
EF_0377 |
Enterococcus faecalis | 3hra_a | Q838Q8 | 98.20 | 3.80E-10 | 3.80E-14 | 80.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | ABAYE2397 |
ABAYE2397 |
Acinetobacter baumannii | 5d66_a | B0VB33 | 98.40 | 6.60E-11 | 6.50E-15 | 85.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | ILK ILK1 ILK2 |
Integrin-linked protein kinase (EC 2.7.11.1) (59 kDa serine/threonine-protein kinase) (Beta-integrin-linked kinase) (ILK-1) (ILK-2) (p59ILK) |
2.7.11.1 | Homo sapiens | Polycystic Kidney Disease,Thyroid Gland Anaplastic Carcinoma,Hypertrophic Cardiomyopathy,Dilated Cardiomyopathy,Hypermobile Ehlers-Danlos Syndrome,Focal Segmental Glomerulosclerosis,Brain Cancer,Ovarian Cancer,Colorectal Cancer,Prostate Cancer,Hyperphosphatemia,Exudative Vitreoretinopathy,Renal Fibrosis,Lung Cancer,Pancreatic Cancer |
2kbx_a | Q13418 | ENSG00000166333 | ILK | 98.00 | 2.10E-09 | 2.10E-13 | 75.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL239W | YAR1 | SGDID:S000006160 | TV1425 TVG1472127 |
Putative ankyrin repeat protein TV1425 |
Thermoplasma volcanium | 2rfm_b | Q978J0 | 98.30 | 1.10E-10 | 1.10E-14 | 84.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | SWH1 OSH1 YAR042W YAR044W |
Oxysterol-binding protein homolog 1 |
Saccharomyces cerevisiae | 5h28_a | P35845 | 98.00 | 1.70E-09 | 1.60E-13 | 81.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | Bd3460 |
Bd3460 |
Bdellovibrio bacteriovorus | 5cer_j | Q6MHS9 | 98.10 | 9.40E-10 | 9.40E-14 | 78.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | ANK2 ANKB |
Ankyrin-2 (ANK-2) (Ankyrin-B) (Brain ankyrin) (Non-erythroid ankyrin) |
Homo sapiens | Timothy Syndrome,Heart Disease,Hypertrophic Cardiomyopathy,Familial Long Qt Syndrome,Legionnaire Disease,Long Qt Syndrome 12,Dilated Cardiomyopathy,Jervell And Lange-Nielsen Syndrome 1,Hereditary Spherocytosis,Long Qt Syndrome,Heart Conduction Disease,Progressive Familial Heart Block, Type Ia,Sick Sinus Syndrome,Andersen Cardiodysrhythmic Periodic Paralysis,Cardiac Arrhythmia,Developmental And Epileptic Encephalopathy 5,Long Qt Syndrome 13,Disease Of Mental Health,Long Qt Syndrome 3,Long Qt Syndrome 2,Long Qt Syndrome 6,Long Qt Syndrome 5,Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Long Qt Syndrome 9,Long Qt Syndrome 10,Long Qt Syndrome 11,Coffin-Siris Syndrome 1,Brugada Syndrome 3,Familial Atrial Fibrillation,Sinoatrial Node Disease,Long Qt Syndrome 1,Intrinsic Cardiomyopathy,Autism Spectrum Disorder,Atrial Fibrillation,Cardiac Arrest,Autism,Catecholaminergic Polymorphic Ventricular Tachycardia,Spinocerebellar Ataxia 5,Cardiac Arrhythmia, Ankyrin-B-Related |
4rly_a | Q01484 | ENSG00000145362 | ANK2 | 98.10 | 8.10E-10 | 8.10E-14 | 85.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL239W | YAR1 | SGDID:S000006160 | ASB9 |
Ankyrin repeat and SOCS box protein 9 (ASB-9) |
Homo sapiens | Uterine Corpus Endometrial Carcinoma |
3zkj_a | Q96DX5 | ENSG00000102048 | ASB9 | 98.10 | 1.20E-09 | 1.20E-13 | 82.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL239W | YAR1 | SGDID:S000006160 | PSMD10 |
26S proteasome non-ATPase regulatory subunit 10 (26S proteasome regulatory subunit p28) (Gankyrin) (p28(GANK)) |
Homo sapiens | Dedifferentiated Liposarcoma,Hepatocellular Carcinoma,Retinoblastoma |
5vhi_g | O75832 | ENSG00000101843 | PSMD10 | 98.10 | 6.80E-10 | 6.70E-14 | 81.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL239W | YAR1 | SGDID:S000006160 | KLLA0_C04147g |
KLLA0_C04147g |
Kluyveromyces lactis | 5h2a_a | Q6CUK7 | 98.20 | 5.60E-10 | 5.40E-14 | 86.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YPL239W | YAR1 | SGDID:S000006160 | Shank3 Prosap2 |
SH3 and multiple ankyrin repeat domains protein 3 (Shank3) (Proline-rich synapse-associated protein 2) (ProSAP2) (SPANK-2) |
Rattus norvegicus | 5g4x_a | Q9JLU4 | 98.10 | 1.10E-09 | 1.00E-13 | 87.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |