Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "V"
51 to 60 of 129 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

51
Vasoactive intestinal peptide receptor 1
HVR1, II, PACAP-R-2, PACAP-R2, RDC1, V1RG, VAPC1, VIP-R-1, VIPR, VIRG, VPAC1, VPAC1R, VPCAP1R
Bipolar disorder, Hepatocellular carcinoma, Diverticular disease, Esophageal achalasia, Metabolic syndrome, Obesity, Diabetes mellitus type 2

52
Vasoactive intestinal peptide receptor 2
C16DUPq36.3, DUP7q36.3, PACAP-R-3, PACAP-R3, VIP-R-2, VPAC2, VPAC2R, VPCAP2R
Alzheimer disease, Bipolar disorder, Corneal astigmatism, Gastroesophageal reflux disease, Schizophrenia

53
Vitrin
VIT1
Cerebral artery occlusion, Hypertrophic cardiomyopathy, Metabolic syndrome, Oligodendroglioma, Osteoarthritis, Ovarian serous carcinoma, Peripheral arterial disease, Schizophrenia, Stroke, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm

54
Vitamin K epoxide reductase complex subunit 1
EDTP308, MST134, MST576, VKCFD2, VKOR
Aortic rupture, Blood coagulation disorder, Cerebrovascular disorder, Coronary artery disease, Coumarin resistance, Hemorrhage, Stroke, Thrombosis, Vascular disease, Venous thromboembolism, Combined deficiency of vitamin k-dependent clotting factors

55
Vitamin K epoxide reductase complex subunit 1L1
-
Keratoconus

56
Very low density lipoprotein receptor
CAMRQ1, CARMQ1, CHRMQ1, VLDL-R, VLDLRCH
Alzheimer disease, Autism, Autoimmune thrombocytopenic purpura, Breast cancer, Cerebellar ataxia, impaired intellectual development, and dysequilibrium, Cerebellar ataxia, intellectual disability, and dysequilibrium, Cerebellar hypoplasia, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Congenital neurologic anomalies, Dysequilibrium syndrome, Intellectual developmental disorder, Nonalcoholic fatty liver disease, Obesity, Schizophrenia

57
Vacuolar ATPase assembly factor VMA12
C17orf32, CDG2P, TMEM199, VPH2
Congenital disorder of glycosylation

58
Vacuolar ATPase assembly factor VMA21
MEAX, XMEA
X-linked myopathy

59
Vacuolar ATPase assembly factor VMA22
CCDC115, CDG2O, ccp1
Congenital disorder of glycosylation

60
Vitelline membrane outer layer 1 homolog
ERGA6350, PRO21055
Renal cell carcinoma