14771
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WSC domain containing 2 |
- |
Attention deficit hyperactivity disorder, Bipolar disorder, Color vision deficiency, Diabetes mellitus, Lung cancer, Metabolic syndrome, Osteoarthritis, Parkinson disease, Pelvic organ prolapse, Periprosthetic osteolysis, Prostate cancer, Schizophrenia, Squamous cell carcinoma, Substance abuse, Diabetes mellitus type 2 |
14772
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|
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WT1 transcription factor |
AWT1, GUD, NPHS4, WAGR, WIT-2, WT-1, WT33 |
11p partial monosomy syndrome, Alzheimer disease, Ambiguous genitalia, Aniridia, Breast neoplasms, Cholelithiasis, Kidney disease, Colonic neoplasms, Color vision deficiency, Congenital aniridia, Coronary artery disease, Denys drash syndrome, Desmoplastic small round cell tumor, Drash syndrome, Endometriosis, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Fraser syndrome, Gastroesophageal reflux disease, Genetic steroid-resistant nephrotic syndrome, Glioblastoma, Glomerulonephritis, Gonadal dysgenesis, Hereditary steroid-resistant nephrotic syndrome, Leber congenital amaurosis, Leukemia, Myeloid leukemia, Promyelocytic leukemia, Lung neoplasms, Male infertility single gene azoospermia, Mesothelioma, Nephrotic syndrome, Osteosarcoma, Premature ovarian failure, Pancreatic neoplasms, Pelvic organ prolapse, Peritoneal neoplasms, Steroid-resistant nephrotic syndrome, Diabetes mellitus type 2, Uterine fibroid, Uterine prolapse, Wagr syndrome, Wilms tumorView all (28 more) |
14773
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WT1 associated protein |
Mum2 |
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14774
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WW and C2 domain containing 1 |
HBEBP3, HBEBP36, KIBRA, MEMRYQTL, PPP1R168 |
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14775
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WW domain containing oxidoreductase |
D16S432E, DEE28, EIEE28, FOR, FRA16D, HHCMA56, PRO0128, SCAR12, SDR41C1, WOX1 |
46,xy partial gonadal dysgenesis, Alzheimer disease, Anorexia nervosa, Juvenile arthritis, Astrocytoma, Spinocerebellar ataxia, Autism, Cerebellar ataxia, Bipolar disorder, Brain atrophy, Breast cancer, Breast neoplasms, Squamous cell carcinoma, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Congenital neurologic anomalies, Crohn disease, Developmental and epileptic encephalopathy, Developmental delay, Dilated cardiomyopathy, Eating disorder, Epilepsy, Rolandic epilepsy, Esophageal cancer, Esophageal neoplasms, Esophageal squamous cell carcinoma, Global developmental delay, Inflammatory bowel disease, Insomnia, Intellectual developmental disorder, Juvenile idiopathic arthritis, Major depressive disorder, Multinodular goiter, Multiple sclerosis, Obesity, Oligodendroglioma, Osteoarthritis, Parkinson disease, Oligoarticular juvenile idiopathic arthritis, Pelvic organ prolapse, Peripheral arterial disease, Retinal detachment, Retinopathy, Rheumatic disease, Schizophrenia, Scoliosis, Stomach neoplasms, Stroke, Thrombophilia, Ulcerative colitis, Urologic neoplasms, Venous thromboembolism, West syndromeView all (39 more) |
14776
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WW domain containing E3 ubiquitin protein ligase 1 |
AIP5, Tiul1, hSDRP1 |
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14777
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WW domain containing E3 ubiquitin protein ligase 2 |
AIP2, WWp2-like |
Atherosclerosis, Cataract, Coronary artery disease, Diverticular disease, Heart disease, Hypertension, Irritable bowel syndrome, Myocardial infarction, Myocardial ischemia, Osteoarthritis, Schizophrenia, Spondyloepiphyseal dysplasia, Synovitis, Synovial disorder, Diabetes mellitus type 2 |
14778
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WW domain containing transcription regulator 1 |
TAZ |
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14779
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|
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XPA binding protein 2 |
HCNP, HCRN, NTC90, SYF1 |
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14780
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|
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XIAP associated factor 1 |
BIRC4BP, HSXIAPAF1, XIAPAF1 |
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