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 129 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

81
VPS37A subunit of ESCRT-I
HCRP1, PQBP2, SPG53
Spastic paraplegia, Paraplegia, Hereditary spastic paraplegia

82
VPS37B subunit of ESCRT-I
-
Atrial fibrillation, Insomnia

83
VPS37C subunit of ESCRT-I
-
Breast neoplasms, Hypothyroidism, Rheumatoid arthritis, Scoliosis

84
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)

85
VPS39 subunit of HOPS complex
TLP, VAM6, hVam6p
Breast neoplasms, Cerebellar ataxia, Schizophrenia

86
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

87
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

88
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

89
Vacuolar protein sorting 4 homolog B
MIG1, SKD1, SKD1B, VPS4-2
Dentin dysplasia

90
VPS50 subunit of EARP/GARPII complex
CCDC132, NEDMSC, VPS54L
Amenorrhea, Neurodevelopmental disorder, Psychiatric disorders