Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "V"
51 to 60 of 131 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

51
VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog
C14orf133, SPE-39, SPE39, VIPAR, VPS16B, hSPE-39
Arthrogryposis-renal dysfunction-cholestasis syndrome

52
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, Liver cirrhosis, Metabolic syndrome, Obesity, Diabetes mellitus type 2

53
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

54
Vitrin
VIT1
Cerebral artery occlusion, Hypertrophic cardiomyopathy, Leprosy, Metabolic syndrome, Oligodendroglioma, Osteoarthritis, Ovarian serous carcinoma, Peripheral arterial disease, Schizophrenia, Stroke, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm

55
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 vitamin k-dependent clotting factor deficiency

56
Vitamin K epoxide reductase complex subunit 1L1
-
Keratoconus

57
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

58
Vacuolar ATPase assembly factor VMA12
C17orf32, CDG2P, TMEM199, VPH2
Congenital disorder of glycosylation

59
Vacuolar ATPase assembly factor VMA21
MEAX, XMEA
X-linked myopathy

60
Vacuolar ATPase assembly factor VMA22
CCDC115, CDG2O, ccp1
Congenital disorder of glycosylation