Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14651 to 14660 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14651
Vitelline membrane outer layer 1 homolog
ERGA6350, PRO21055
Renal cell carcinoma

14652
Vacuole membrane protein 1
EPG3, TANGO5, TMEM49
Breast cancer, Lymphocytic leukemia, Dilated cardiomyopathy, Gout, Major depressive disorder, Multiple sclerosis, Uterine fibroid

14653
Vomeronasal 1 receptor 5 (gene/pseudogene)
V1RL5
Glioma, Vascular dementia

14654
Vanin 1
HDLCQ8, Tiff66
Celiac disease, Colorectal cancer, Atopic dermatitis, Dyslipidemias, Inflammatory bowel disease, Psoriasis

14655
Vanin 2
FOAP-4, GPI-80
Atopic dermatitis, Major depressive disorder, Psoriasis

14656
VOPP1 WW domain binding protein
ECOP, GASP, WBP1L2
Myeloid leukemia, Liver cirrhosis

14657
V-set pre-B cell surrogate light chain 1
CD179a, IGI, IGVPB, VPREB
Alzheimer disease

14658
VPS11 core subunit of CORVET and HOPS complexes
DYT32, END1, HLD12, HLD12; DYT32, PEP5, RNF108, hVPS11
Coronary artery disease, Dystonia, Gallstones, Hypomyelinating leukodystrophy, Diabetes mellitus type 2

14659
Vacuolar protein sorting 13 homolog A
BLTP5A, CHAC, CHOREIN
Benign hereditary chorea, Chorea, Choreoacanthocytosis, Congenital neurologic anomalies, Vascular dementia, Mood disorder

14660
Vacuolar protein sorting 13 homolog B
BLTP5B, CHS1, COH1
Attention deficit hyperactivity disorder, Autism, Central nervous system cancer, Cholecystolithiasis, Ciliary dyskinesia, Cohen syndrome, Congenital neurologic anomalies, Dental caries, Endometriosis, Long qt syndrome, Glioblastoma, Glioma, Global developmental delay, Intellectual developmental disorder, Lung cancer
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