Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14671 to 14680 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14671
Vacuolar protein sorting 36 homolog
C13orf9, CGI-145, EAP45
Lewy body disease

14672
VPS37A subunit of ESCRT-I
HCRP1, PQBP2, SPG53
Spastic paraplegia, Paraplegia, Hereditary spastic paraplegia

14673
VPS37B subunit of ESCRT-I
-
Atrial fibrillation, Insomnia

14674
VPS37C subunit of ESCRT-I
-
Breast neoplasms, Hypothyroidism, Rheumatoid arthritis, Scoliosis

14675
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
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14676
VPS39 subunit of HOPS complex
TLP, VAM6, hVam6p
Breast neoplasms, Cerebellar ataxia, Schizophrenia

14677
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

14678
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

14679
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

14680
Vacuolar protein sorting 4 homolog B
MIG1, SKD1, SKD1B, VPS4-2
Dentin dysplasia