Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "V"

21 to 30 of 131 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
21	7410	VAV2	Vav guanine nucleotide exchange factor 2	VAV-2	Alzheimer disease, Central nervous system cancer, Colorectal cancer, Corneal astigmatism, Dementia, Glaucoma, Glioblastoma, Glioma, Multiple sclerosis, Nonalcoholic fatty liver disease, Open angle glaucoma, Prostate cancer, Diabetes mellitus type 2
22	10451	VAV3	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 View all (2 more)
23	11023	VAX1	Ventral anterior homeobox 1	MCOPS11	Anophthalmia/microphthalmia-esophageal atresia syndrome, Microphthalmia, Microphthalmos
24	25806	VAX2	Ventral anterior homeobox 2	DRES93	Color vision deficiency, Corneal astigmatism, Gout, Scoliosis
25	7411	VBP1	VHL binding protein 1	HIBBJ46, PFD3, PFDN3, VBP-1	Venous thromboembolism
26	7412	VCAM1	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 View all (5 more)
27	1462	VCAN	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 View all (3 more)
28	84923	VCF1	VCP nuclear cofactor family member 1	FAM104A	Congenital disorder of glycosylation
29	90736	VCF2	VCP nuclear cofactor family member 2	CXorf44, FAM104B	Androgenetic alopecia
30	7414	VCL	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

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