Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14601 to 14610 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14601
VPS26 endosomal protein sorting factor C
DCRA, DSCR3, DSCRA
Neurodevelopmental disorder, Oligodendroglioma, Diabetes mellitus type 2

14602
VPS33A core subunit of CORVET and HOPS complexes
MPSPS
Desbuquois syndrome, Mucopolysaccharidosis

14603
VPS33B late endosome and lysosome associated
KDIDAR, PFIC12
Arthrogryposis multiplex congenita, Arthrogryposis-renal dysfunction-cholestasis syndrome, Cholelithiasis, Kidney disease, Coronary artery disease, Hypertension, Insomnia, Metabolic syndrome, Myocardial infarction, Progressive intrahepatic cholestasis, Willis-ekbom disease, Stroke, Thrombocytopenia, Diabetes mellitus type 2

14604
VPS35 retromer complex component
MEM3, PARK17
Parkinson disease, Ear, patella, short stature syndrome, Hereditary parkinson disease, Intellectual developmental disorder, Schizophrenia

14605
VPS35 endosomal protein sorting factor like
C16orf62, EC97, RTSC3
Barrett esophagus, Desbuquois syndrome, Gastric cancer, Insomnia, Myocardial infarction, Obstructive sleep apnea syndrome, Ritscher-schinzler syndrome

14606
Vacuolar protein sorting 36 homolog
C13orf9, CGI-145, EAP45
Lewy body disease

14607
VPS37A subunit of ESCRT-I
HCRP1, PQBP2, SPG53
Spastic paraplegia, Paraplegia, Hereditary spastic paraplegia

14608
VPS37B subunit of ESCRT-I
-
Atrial fibrillation, Insomnia

14609
VPS37C subunit of ESCRT-I
-
Breast neoplasms, Hypothyroidism, Rheumatoid arthritis, Scoliosis

14610
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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