Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "V"

81 to 90 of 99 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
81	7444	VRK2	VRK serine/threonine kinase 2	-	Congenital intestinal aganglionosis, Development disorder, Fanconi anemia, Hirschsprung disease, Mental depression, Mood disorder, Psychosis, Schizophrenia
82	7447	VSNL1	Visinin like 1	HLP3, HPCAL3, HUVISL1, VILIP, VILIP-1	Alzheimer disease, Diabetes mellitus, Schizophrenia, Senile dementia, Transient psychotic disorder
83	7448	VTN	Vitronectin	V75, VN, VNT	Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Hemolytic uremic syndrome, Ileocolitis, Liver cirrhosis, Liver fibrosis
84	7450	VWF	Von Willebrand factor	F8VWF, VWD	Aortic valve sclerosis, Atrial fibrillation, Breast cancer, Cardiovascular diseases, Cerebral thrombosis, Cerebral thrombus, Congestive heart failure, Gastrointestinal angiodysplasia, Heart failure, Hypertension, Intracranial thrombosis, Mitral valve prolapse, Multiple congenital anomalies, Myocardial infarction, Paroxysmal atrial fibrillation View all (2 more)
85	79001	VKORC1	Vitamin K epoxide reductase complex subunit 1	EDTP308, MST134, MST576, VKCFD2, VKOR	Aortic aneurysm, Aortic rupture, Blood coagulation disorders, Combined deficiency of vitamin k-dependent clotting factors, Coronary heart disease, Stroke, Vascular diseases
86	79679	VTCN1	V-set domain containing T cell activation inhibitor 1	B7-H4, B7H4, B7S1, B7X, B7h.5, PRO1291, VCTN1	Arthritis
87	80737	VWA7	Von Willebrand factor A domain containing 7	C6orf27, G7c, NG37	Crohn disease, Diabetes mellitus, Hodgkin disease, Lupus erythematosus, Rheumatoid arthritis
88	81552	VOPP1	VOPP1 WW domain binding protein	ECOP, GASP, WBP1L2	Leukemia, Myeloid leukemia, Myocardial infarction
89	81671	VMP1	Vacuole membrane protein 1	EPG3, TANGO5, TMEM49	B-cell lymphoma, Lymphocytic leukemia, Multiple sclerosis
90	81839	VANGL1	VANGL planar cell polarity protein 1	KITENIN, LPP2, STB2, STBM2	Acrania, Ambiguous genitalia, Anencephaly, Arnold-chiari malformation, Arrhinencephaly, Bowel incontinence, Caudal regression sequence, Cervical spina bifida aperta, Cervical spina bifida cystica, Cervicothoracic spina bifida, Congenital clubfoot, Pulmonary hypoplasia, Congenital meningocele, Craniorachischisis, Cryptorchidism View all (33 more)

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