14551
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Vascular cell adhesion molecule 1 |
CD106, INCAM-100 |
Sickle cell anemia, Arteriosclerosis, Atherosclerosis, Hepatocellular carcinoma, Cardiovascular disease, Cholelithiasis, Ulcerative colitis, Dermatitis, Digestive system disease, Hypercholesterolemia, Hypertension, Intrahepatic cholestasis of pregnancy, Multiple sclerosis, Myocardial ischemia, Open angle glaucoma, Primary graft dysfunction, Prostate cancer, Schizophrenia, Uremia, UrticariaView all (5 more) |
14552
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|
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Versican |
CSPG2, ERVR, GHAP, PG-M, WGN, WGN1 |
Asthma, Adenoid cystic carcinoma, Basal cell carcinoma, Carpal tunnel syndrome, Colorectal cancer, Diverticular disease, Endometriosis, Gastroesophageal reflux disease, Intracranial aneurysm, Laryngeal carcinoma, Major depressive disorder, Marshall syndrome, Psychiatric disorders, Retinitis pigmentosa, Salivary gland neoplasms, Stickler syndrome, Vitreoretinal degeneration, Wagner syndromeView all (3 more) |
14553
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|
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VCP nuclear cofactor family member 1 |
FAM104A |
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14554
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|
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VCP nuclear cofactor family member 2 |
CXorf44, FAM104B |
|
14555
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|
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Vinculin |
CMD1W, CMH15, HEL114, MV, MVCL, VINC |
Autism, Cardiomyopathy, Dilated cardiomyopathy, Color vision deficiency, Congestive heart failure, Hirschsprung disease, Hypertrophic cardiomyopathy, Long qt syndrome, Osteoporosis, Short qt syndrome, Ventricular fibrillation, Wolff-parkinson-white syndrome |
14556
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|
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Valosin containing protein |
CDC48, FTDALS6, TERA, p97 |
Distal myopathy, Alzheimer disease, Amyotrophic lateral sclerosis, Charcot-marie-tooth disease, Neurodevelopmental disorder, Dejerine-sottas disease, Fanconi anemia, Frontotemporal dementia with or without amyotrophic lateral sclerosis, Frontotemporal dementia with motor neuron disease, Global developmental delay, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Intellectual developmental disorder, Lewy body disease, Myositis, Non-specific syndromic intellectual disability, Peroneal muscle atrophy, Prostatic neoplasms, Roussy-levy syndrome, Spastic paraplegia, Stevens-johnson syndromeView all (6 more) |
14557
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|
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Variable charge Y-linked |
BPY1, VCY1, VCY1A |
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14558
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|
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Voltage dependent anion channel 1 |
PORIN, VDAC-1 |
Asthma, Autoimmune thyroid disease, Cancer, Diabetic neuropathy, Epilepsy, Hypothyroidism, Mitochondrial myopathy, Multiple sclerosis, Myocardial infarction, Open angle glaucoma, Psychiatric disorders, Respiratory system disease, Rheumatoid arthritis, Systemic lupus erythematosus, Ventricular dysfunction |
14559
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|
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Voltage dependent anion channel 2 |
POR |
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14560
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|
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Vitamin D receptor |
NR1I1, PPP1R163 |
Amyotrophic lateral sclerosis, Asthma, Autism, Autoimmune hepatitis, Barrett esophagus, Basal cell carcinoma, Behcet disease, Biliary cirrhosis, Bipolar disorder, Bonnevie-ullrich syndrome, Breast neoplasms, Bronchopulmonary dysplasia, Transitional cell carcinoma, Cardiovascular disease, Ischemic heart disease, Obstructive airway disease, Congenital stenosis of aortic valve, Coronary artery disease, Atopic dermatitis, Desbuquois syndrome, Diabetic retinopathy, Temporal lobe epilepsy, Fabry disease, Hyperparathyroidism, Hypophosphatemic rickets, Fatty liver, Fatty liver, alcoholic, Gout, Graves disease, Hypertension, Hypocalcemic vitamin d-dependent rickets, Lymphocytic b-cell leukemia, Liver cirrhosis, Multiple sclerosis, Myocardial ischemia, Myopia, Parkinson disease, Peptic esophagitis, Polycystic ovary syndrome, Biliary cholangitis, Prostatic neoplasms, Psoriasis, Rheumatoid arthritis, Rickets, Scoliosis, Depression, Turner syndrome, Uremia, Vitamin d deficiency, Vitamin d dependent rickets, VitiligoView all (36 more) |
