Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14701 to 14710 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14701
V-set and transmembrane domain containing 4
C10orf72
Cataract, Diverticular disease, Migraine

14702
V-set and transmembrane domain containing 5
C11orf90
Androgenetic alopecia, Central nervous system cancer, Glioblastoma, Glioma, Intestinal obstruction, Obesity

14703
Visual system homeobox 1
CAASDS, KTCN, KTCN1, PPCD, PPCD1, PPD, RINX
Auditory perceptual disorder, Color vision deficiency, Corneal dystrophy, Craniofacial abnormalities, Craniofacial anomalies with anterior segment dysgenesis, Eye abnormalities, Long qt syndrome, Hereditary corneal dystrophy, Keratoconus, Polymorphous corneal dystrophy, Posterior polymorphous corneal dystrophy

14704
Visual system homeobox 2
CHX10, HOX10, MCOP2, MCOPCB3, RET1
Anophthalmia/microphthalmia-esophageal atresia syndrome, Anophthalmia, Blindness, Breast cancer, Colobomatous microphthalmia, Congenital cystic eyeball, Crohn disease, Inflammatory bowel disease, Microphthalmia, Microphthalmos, Ocular sarcoidosis, Retinitis pigmentosa, Ulcerative colitis

14705
Vesicle trafficking 1
6orf55, C6orf55, DRG-1, DRG1, HSPC228, LIP5, My012, SBP1
Obstructive pulmonary disease, Respiratory system disease

14706
V-set domain containing T cell activation inhibitor 1
B7-H4, B7H4, B7S1, B7X, B7h.5, PRO1291, VCTN1
Coronary artery disease, Juvenile idiopathic arthritis

14707
Vesicle transport through interaction with t-SNAREs 1A
MMDS3, MVti1, VTI1RP2, Vti1-rp2
Alzheimer disease, Atherosclerosis, Attention deficit hyperactivity disorder, Central nervous system cancer, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Dementia, Diabetes mellitus, Glioma, Heart failure, Hypertrophic cardiomyopathy, Immune system disease, Lung cancer, Migraine
View all (6 more)

14708
Vitronectin
V75, VN, VNT
Crohn disease, Granulomatosis with polyangiitis, Hypertension, Liver cirrhosis

14709
Von Willebrand factor A domain containing 1
HMNMYO, HMNR7, WARP
Neuromuscular disease, Distal hereditary motor neuropathy

14710
Von Willebrand factor A domain containing 2
AMACO, CCSP-2, CCSP2, NET42
Congenital anomalies of the kidney and urinary tract, Congenital anomalies of kidney and urinary tract, Oligodendroglioma, Vesicoureteral reflux