Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "V"

21 to 30 of 99 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
21	23230	VPS13A	Vacuolar protein sorting 13 homolog A	BLTP5A, CHAC, CHOREIN	Abetalipoproteinemia, Anxiety disorder, Attention deficit hyperactivity disorder, Cataract, Cerebral cortical atrophy, Chorea, Choreoacanthocytosis, Colorectal cancer, Developmental regression, Distal muscular atrophy, Dwarfism, Dysarthria, Dysgraphia, Dysphagia, Dyssomnia View all (15 more)
22	23339	VPS39	VPS39 subunit of HOPS complex	TLP, VAM6, hVam6p	Breast cancer, Mammary neoplasms, Breast carcinoma, Marfan syndrome, Schizophrenia
23	23355	VPS8	VPS8 subunit of CORVET complex	KIAA0804	Arthrogryposis multiplex congenita
24	245806	VGLL2	Vestigial like family member 2	VGL2, VITO1	Melanoma
25	25806	VAX2	Ventral anterior homeobox 2	DRES93	Astigmatism, Corneal astigmatism, Dysmorphic features, Multiple congenital anomalies, Nephrocalcinosis, Nephrolithiasis, Renal tubular acidosis, distal, with progressive nerve deafness
26	26276	VPS33B	VPS33B late endosome and lysosome associated	KDIDAR, PFIC12	Arthrogryposis multiplex congenita, Arthrogryposis, renal dysfunction, and cholestasis, Atrial septal defect, Cholestatic liver disease, Congenital anomalies of kidney and urinary tract, Conjugated hyperbilirubinemia, Developmental delay, Diabetes mellitus, Ichthyosis, Kidney disease, Microcephaly, Micrognathism, Multiple congenital anomalies, Nephrocalcinosis, Vacuolar myopathy View all (2 more)
27	27072	VPS41	VPS41 subunit of HOPS complex	HVPS41, HVSP41, SCAR29, hVps41p	Mental depression
28	27287	VENTX	VENT homeobox	HPX42B, NA88A, VENTX2	Esophagus neoplasm
29	284013	VMO1	Vitelline membrane outer layer 1 homolog	ERGA6350, PRO21055	Chromophobe carcinoma, Papillary renal carcinoma, Renal carcinoma
30	30813	VSX1	Visual system homeobox 1	CAASDS, KTCN, KTCN1, PPCD, PPCD1, PPD, RINX	Astigmatism, Auditory processing disorder, Corneal endothelial dystrophy, Corneal granular dystrophy, Craniofacial anomalies and anterior segment dysgenesis syndrome, Empty sella syndrome, Encephalocele, Groenouw`s dystrophies, Hereditary corneal dystrophy, Hydrocephalus, Isolated keratoconus, Keratoconus, Macular corneal dystrophy, Polymorphous corneal dystrophy, Retinal diseases, Stromal corneal dystrophy View all (1 more)

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