21
|
|
|
Vav guanine nucleotide exchange factor 3 |
- |
Asthma, Auditory system disease, Autoimmune disease, Autoimmune thyroid disease, Differentiated thyroid carcinoma, Graves disease, Hashimoto disease, Hypertension, Hyperthyroidism, Hypothyroidism, Iga nephropathy, Juvenile idiopathic arthritis, Thyroid carcinoma, Prostatic neoplasms, Psoriasis, Seasonal allergic rhinitis, Thyroid diseaseView all (2 more) |
22
|
|
|
Ventral anterior homeobox 1 |
MCOPS11 |
|
23
|
|
|
Ventral anterior homeobox 2 |
DRES93 |
|
24
|
|
|
VHL binding protein 1 |
HIBBJ46, PFD3, PFDN3, VBP-1 |
|
25
|
|
|
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) |
26
|
|
|
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) |
27
|
|
|
VCP nuclear cofactor family member 1 |
FAM104A |
|
28
|
|
|
VCP nuclear cofactor family member 2 |
CXorf44, FAM104B |
|
29
|
|
|
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 |
30
|
|
|
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) |
