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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YGR233C | PHO81 | SGDID:S000003465 | 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 | 98.90 | 1.30E-13 | 1.60E-17 | 132.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGR233C | PHO81 | SGDID:S000003465 | CTHT_0005190 |
CTHT_0005190 |
Chaetomium thermophilum | 5ijj_b | G0RY29 | 98.80 | 5.80E-13 | 5.80E-17 | 133.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGR233C | PHO81 | SGDID:S000003465 | Espn |
Espin (Ectoplasmic specialization protein) |
Mus musculus | 5et1_b | Q9ET47 | 99.30 | 2.10E-16 | 2.70E-20 | 159.10 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YGR233C | PHO81 | SGDID:S000003465 | 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 |
5y4d_a | Q01484 | ENSG00000145362 | ANK2 | 99.10 | 3.90E-15 | 4.80E-19 | 166.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGR233C | PHO81 | SGDID:S000003465 | nompC CG17468 CT30855 Dmel\CG11020 DmNompC jf24 l(2)25Dc l(2)jf24 nomp NOMPC NompC ORE-13 TRPN TRPN1 CG11020 Dmel_CG11020 |
nompC CG17468 CT30855 Dmel\CG11020 DmNompC jf24 l(2)25Dc l(2)jf24 nomp NOMPC NompC ORE-13 TRPN TRPN1 CG11020 Dmel_CG11020 |
Drosophila melanogaster | 5vkq_d | E0A9E1 | 99.20 | 3.10E-15 | 3.50E-19 | 189.40 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YGR233C | PHO81 | SGDID:S000003465 | 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 | 99.20 | 9.00E-16 | 1.20E-19 | 144.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YGR233C | PHO81 | SGDID:S000003465 | NAS6 YGR232W G8564 |
Probable 26S proteasome regulatory subunit p28 (Proteasome non-ATPase subunit 6) |
Saccharomyces cerevisiae | 1wg0_a | P50086 | 99.00 | 6.60E-14 | 8.40E-18 | 131.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGR233C | PHO81 | SGDID:S000003465 | 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 | 99.10 | 5.60E-15 | 6.20E-19 | 147.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YGR233C | PHO81 | SGDID:S000003465 | K1L |
K1L |
Vaccinia virus | 3kea_b | Q6IV60 | 98.90 | 2.00E-13 | 2.50E-17 | 132.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGR233C | PHO81 | SGDID:S000003465 | 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 | 99.20 | 5.70E-16 | 7.20E-20 | 161.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YGR233C | PHO81 | SGDID:S000003465 | XPR1 SYG1 XR |
Xenotropic and polytropic retrovirus receptor 1 (Protein SYG1 homolog) (Xenotropic and polytropic murine leukemia virus receptor X3) (X-receptor) |
Homo sapiens | Basal Ganglia Disease,Leukemia,Dystonia,Fanconi Syndrome,Basal Ganglia Calcification, Idiopathic, 6,Basal Ganglia Calcification,Basal Ganglia Calcification, Idiopathic, 1 |
5ijh_b | Q9UBH6 | ENSG00000143324 | XPR1 | 99.20 | 1.50E-15 | 1.60E-19 | 153.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGR233C | PHO81 | SGDID:S000003465 | legA1 lpg2416 |
legA1 lpg2416 |
Legionella pneumophila | 2aja_b | Q5ZSV0 | 99.00 | 6.80E-14 | 8.20E-18 | 145.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGR233C | PHO81 | SGDID:S000003465 | MACROH2A1 H2AFY |
Core histone macro-H2A.1 (Histone macroH2A1) (mH2A1) (Histone H2A.y) (H2A/y) (Medulloblastoma antigen MU-MB-50.205) |
Homo sapiens | Breast Cancer,Fanconi Anemia, Complementation Group A,Liebenberg Syndrome,Medulloblastoma |
5iit_a | O75367 | ENSG00000113648 | MACROH2A1 | 98.80 | 3.70E-13 | 4.00E-17 | 145.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGR233C | PHO81 | SGDID:S000003465 | 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 | 99.00 | 3.60E-14 | 4.70E-18 | 132.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YGR233C | PHO81 | SGDID:S000003465 | RNASEL RNS4 |
2-5A-dependent ribonuclease (2-5A-dependent RNase) (EC 3.1.26.-) (Ribonuclease 4) (Ribonuclease L) (RNase L) |
3.1.26.- | Homo sapiens | Viral Infectious Disease,Myalgic Encephalomyelitis/Chronic Fatigue Syndrome,Rasopathy,Dengue Disease,Prostate Cancer, Hereditary, 1,West Nile Encephalitis,West Nile Fever,Noonan Syndrome 1,Chronic Fatigue Syndrome,Herpes Simplex,West Nile Virus Infection,Vaccinia,Prostate Cancer,Lynch Syndrome,La Crosse Encephalitis,Noonan Syndrome 2,Paralytic Poliomyelitis,Aicardi-Goutieres Syndrome,Immune Deficiency Disease,Microphthalmia With Limb Anomalies |
1wdy_a | Q05823 | ENSG00000135828 | RNASEL | 99.40 | 6.80E-18 | 9.00E-22 | 161.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YGR233C | PHO81 | SGDID:S000003465 | LMJF_29_1100 |
LMJF_29_1100 |
Leishmania major | 3ljn_a | E9ADW8 | 99.30 | 7.30E-17 | 9.30E-21 | 162.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGR233C | PHO81 | SGDID:S000003465 | ASB11 |
Ankyrin repeat and SOCS box protein 11 (ASB-11) |
Homo sapiens | Lacrimal Duct Obstruction |
4uuc_a | Q8WXH4 | ENSG00000165192 | ASB11 | 99.10 | 6.00E-15 | 7.90E-19 | 135.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGR233C | PHO81 | SGDID:S000003465 | NFKB2 LYT10 |
Nuclear factor NF-kappa-B p100 subunit (DNA-binding factor KBF2) (H2TF1) (Lymphocyte translocation chromosome 10 protein) (Nuclear factor of kappa light polypeptide gene enhancer in B-cells 2) (Oncogene Lyt-10) (Lyt10) [Cleaved into: Nuclear factor NF-kappa-B p52 subunit] |
Homo sapiens | Immunodeficiency 10,B Cell Deficiency,Ectodermal Dysplasia,B-Cell Non-Hodgkin Lymphoma,B-Cell Lymphoma,Common Variable Immunodeficiency,Asbestos-Related Lung Carcinoma,Combined Immunodeficiency,Legionellosis,Osteopetrosis,Neuroaspergillosis,Immunodeficiency, Common Variable, 10,Splenic Marginal Zone Lymphoma,Lymphoma,Acth Deficiency, Isolated,Incontinentia Pigmenti,Immunodeficiency, Common Variable, 1 |
4ot9_a | Q00653 | ENSG00000077150 | NFKB2 | 99.00 | 2.60E-14 | 3.30E-18 | 143.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGR233C | PHO81 | SGDID:S000003465 | 85/88 kDa calcium-independent phospholipase A2 (CaI-PLA2) (EC 3.1.1.4) (2-lysophosphatidylcholine acylhydrolase) (EC 3.1.1.5) (Group VI phospholipase A2) (GVI PLA2) (Intracellular membrane-associated calcium-independent phospholipase A2 beta) (iPLA2-beta) (PLA2G6) (Palmitoyl-CoA hydrolase) (EC 3.1.2.2) (Patatin-like phospholipase domain-containing protein 9) (PNPLA9) |
Cricetulus griseus | 6aun_a | A0A384E119 | 99.00 | 2.90E-14 | 3.40E-18 | 164.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
YGR233C | PHO81 | SGDID:S000003465 | 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 | 99.20 | 4.80E-16 | 6.20E-20 | 154.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YGR233C | PHO81 | SGDID:S000003465 | lin-12 R107.8 |
Protein lin-12 (Abnormal cell lineage protein 12) (Notch-like protein lin-12) |
Caenorhabditis elegans | 2fo1_e | P14585 | 99.20 | 2.70E-15 | 3.40E-19 | 152.00 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
YGR233C | PHO81 | SGDID:S000003465 | Nfkbib Ikbb |
NF-kappa-B inhibitor beta (NF-kappa-BIB) (I-kappa-B-beta) (IkB-B) (IkB-beta) (IkappaBbeta) |
Mus musculus | 1k3z_d | Q60778 | 99.00 | 2.30E-14 | 3.00E-18 | 137.80 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YGR233C | PHO81 | SGDID:S000003465 | 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 | 98.90 | 1.30E-13 | 1.70E-17 | 128.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGR233C | PHO81 | SGDID:S000003465 | 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 | 99.10 | 1.40E-14 | 1.70E-18 | 146.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |