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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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YDR143C | SAN1 | SGDID:S000002550 | Stub1 Chip |
E3 ubiquitin-protein ligase CHIP (EC 2.3.2.27) (Carboxy terminus of Hsp70-interacting protein) (RING-type E3 ubiquitin transferase CHIP) (STIP1 homology and U box-containing protein 1) |
2.3.2.27 | Mus musculus | 2c2l_c | Q9WUD1 | 95.40 | 0.00012 | 2.00E-08 | 55.90 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YDR143C | SAN1 | SGDID:S000002550 | BRCA1 RNF53 |
Breast cancer type 1 susceptibility protein (EC 2.3.2.27) (RING finger protein 53) (RING-type E3 ubiquitin transferase BRCA1) |
2.3.2.27 | Homo sapiens | Cancerophobia,Skin Melanoma,Ovarian Carcinosarcoma,Uterine Carcinosarcoma,Endometrial Cancer,Peritoneum Cancer,Endosalpingiosis,Ganglioneuroblastoma,Breast-Ovarian Cancer, Familial 2,Retinitis Pigmentosa,Adenoid Cystic Carcinoma,Cowden Syndrome,Cowden Syndrome 1,Primary Peritoneal Carcinoma,Cervical Adenoma Malignum,Fallopian Tube Disease,Fallopian Tube Carcinoma,Bilateral Breast Cancer,Synchronous Bilateral Breast Carcinoma,B-Lymphoblastic Leukemia/Lymphoma,Uterine Corpus Cancer,B-Lymphoblastic Leukemia/Lymphoma With Hyperdiploidy,Dysgerminoma,Alzheimer Disease,Familiar Ovarian Carcinoma,Basaloid Lung Carcinoma,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,Hereditary Site-Specific Ovarian Cancer Syndrome,Familial Ovarian Cancer,Amelogenesis Imperfecta,Ovarian Serous Cystadenofibroma,Female Reproductive System Disease,Neuroblastoma,Inherited Cancer-Predisposing Syndrome,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Cystinuria,Thoracic Cancer,Canavan Disease,Papillary Serous Adenocarcinoma,Cystadenoma,Intracystic Papillary Adenoma,Mulchandani-Bhoj-Conlin Syndrome,Dysplastic Nevus Syndrome,Bladder Cancer,Fallopian Tube Clear Cell Adenocarcinoma,Cerebellar Disease,Endocrine System Disease,Deafness, Autosomal Dominant 13,Fanconi Anemia, Complementation Group J,Ovarian Serous Adenofibroma,Cockayne Syndrome,Tetraploidy,Aplastic Anemia,Ovarian Cancer,Adenocarcinoma,In Situ Carcinoma,Female Reproductive Endometrioid Cancer,Breast Ductal Carcinoma,Lobular Neoplasia,Breast Carcinoma In Situ,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Colorectal Cancer,Hypertrophy Of Breast,Endometrial Serous Adenocarcinoma,Cystadenocarcinoma,Papillary Adenocarcinoma,Serous Cystadenocarcinoma,Premature Menopause,Microcephaly,Rhabdomyosarcoma,Werner Syndrome,Ovarian Cystadenoma,Ovarian Disease,Deficiency Anemia,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Palmoplantar Keratoderma, Punctate Type Ii,Skin Carcinoma,Gastric Cancer,Fanconi Anemia, Complementation Group S,Breast Disease,Prostate Cancer,Disease Of Mental Health,Ovarian Cystadenocarcinoma,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Congenital Myasthenic Syndrome,Mutagen Sensitivity,Breast Fibroadenoma,Fallopian Tube Adenocarcinoma,Ovary Adenocarcinoma,Breast-Ovarian Cancer, Familial 1,Ruvalcaba Syndrome,Lynch Syndrome,Lung Squamous Cell Carcinoma,Ovary Transitional Cell Carcinoma,Neural Tube Defects,Fanconi Anemia, Complementation Group D1,Cockayne Syndrome B,Seckel Syndrome,Tooth Agenesis,Body Mass Index Quantitative Trait Locus 20,Riddle Syndrome,Female Breast Cancer,Gastric Cancer, Hereditary Diffuse,Pancreatic Cancer 4,Tumor Predisposition Syndrome,Autosomal Genetic Disease,Ewing Sarcoma,Pigmentary Disorder, Reticulate, With Systemic Manifestations, X-Linked,Nephrolithiasis/Osteoporosis, Hypophosphatemic, 2,Salivary Gland Carcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Ovarian Serous Carcinoma,Autosomal Recessive Cerebellar Ataxia,Nosophobia,Pre-Malignant Neoplasm,Ductal Carcinoma In Situ,Estrogen-Receptor Positive Breast Cancer,Estrogen-Receptor Negative Breast Cancer,Breast Benign Neoplasm,Thoracic Benign Neoplasm,Ovarian Benign Neoplasm,Nijmegen Breakage Syndrome,Li-Fraumeni Syndrome,Ovarian Cancer 1,Punctate Palmoplantar Keratoderma,Myasthenic Syndrome, Congenital, 6, Presynaptic,Ataxia-Telangiectasia,Medulloblastoma,Melanoma, Cutaneous Malignant 1,Melanoma, Uveal,Bloom Syndrome,Primary Autosomal Recessive Microcephaly,Lung Cancer,Pancreatic Cancer |
1jm7_a | P38398 | 95.00 | 0.00033 | 3.60E-08 | 54.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |