Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "V"
81 to 90 of 131 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

81
Vacuolar protein sorting 36 homolog
C13orf9, CGI-145, EAP45
Lewy body disease

82
VPS37A subunit of ESCRT-I
HCRP1, PQBP2, SPG53
Spastic paraplegia, Paraplegia, Hereditary spastic paraplegia

83
VPS37B subunit of ESCRT-I
-
Atrial fibrillation, Insomnia

84
VPS37C subunit of ESCRT-I
-
Breast neoplasms, Hypothyroidism, Rheumatoid arthritis, Scoliosis

85
VPS37D subunit of ESCRT-I
WBSCR24
Atrial fibrillation, Cancer, Basal cell carcinoma, Central nervous system cancer, Cholecystolithiasis, Liver cirrhosis, Coronary artery disease, Diabetes mellitus, Glioblastoma, Glioma, Gout, Heart failure, Metabolic syndrome, Nonalcoholic fatty liver disease, Stroke
View all (2 more)

86
VPS39 subunit of HOPS complex
TLP, VAM6, hVam6p
Breast neoplasms, Cerebellar ataxia, Schizophrenia

87
VPS41 subunit of HOPS complex
HVPS41, HVSP41, SCAR29, hVps41p
Cerebellar ataxia, Breast cancer, Colorectal cancer, Hyper-immunoglobulin d syndrome, Major depressive disorder, Neurotic disorder, Spinocerebellar ataxia

88
Vacuolar protein sorting 45 homolog
H1, H1VPS45, SCN5, VPS45A, VPS45B, VPS54A, VSP45, VSP45A
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Congenital neutropenia, Major depressive disorder, Severe congenital neutropenia, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome

89
Vacuolar protein sorting 4 homolog A
CIMDAG, SKD1, SKD1A, SKD2, VPS4, VPS4-1
Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome, Cimdag syndrome, Intellectual developmental disorder, Metabolic syndrome, Diabetes mellitus type 2

90
Vacuolar protein sorting 4 homolog B
MIG1, SKD1, SKD1B, VPS4-2
Dentin dysplasia