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
14571 to 14580 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14571
Vestigial like family member 4
VGL-4
Androgenetic alopecia, Anorexia nervosa, Atrial fibrillation, Obstructive pulmonary disease, Color vision deficiency, Eating disorder, Insomnia, Osteoarthritis, Stroke

14572
Von Hippel-Lindau tumor suppressor
HRCA1, RCA1, VHL1, pVHL
Au-kline syndrome, Secondary polycythemia, Bullous pemphigoid, Carcinoma, Renal cell carcinoma, Chuvash erythrocytosis, Clear cell renal cell carcinoma, Erythrocytosis due to tissue hypoxemia, Erythrocytosis, Fanconi anemia, Hypertension, Kidney cancer, Kidney neoplasms, Lung neoplasms, Maffucci syndrome
View all (7 more)

14573
Villin 1
D2S1471, VIL
Amyotrophic lateral sclerosis, Cholelithiasis

14574
Vimentin
-
Amyotrophic lateral sclerosis, Atherosclerosis, Behcet disease, Breast neoplasms, Carcinoma, Cataract, Congenital cataract, Degenerative disorder, Hypertrophic cardiomyopathy, Kidney disease, Liver cirrhosis, Systemic lupus erythematosus, Mesothelioma, Motor neuron disease, Nephrotic syndrome
View all (7 more)

14575
Vasoactive intestinal peptide
PHM27
Asperger syndrome, Autism, Bipolar disorder, Bronchial hyperreactivity, Cognition disorder, Delirium, dementia, and cognitive disorders, Down syndrome, Edema, Erectile dysfunction, Hyperalgesia, Hypotension, Intellectual developmental disorder, Prostatic neoplasms, Rhinitis, Sarcoidosis
View all (3 more)

14576
VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog
C14orf133, SPE-39, SPE39, VIPAR, VPS16B, hSPE-39
Arthrogryposis-renal dysfunction-cholestasis syndrome

14577
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

14578
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

14579
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

14580
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