Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "V"
71 to 80 of 129 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

71
Vacuolar protein sorting 13 homolog D
BLTP5D, SCA24, SCAR4, SCASI
Arthrogryposis multiplex congenita, Spinocerebellar ataxia, Cerebellar ataxia, Central nervous system cancer, Cholecystolithiasis, Glioblastoma, Glioma, Non-immune hydrops fetalis, Leigh syndrome, Neurodevelopmental disorder, Pena-shokeir syndrome , Psychiatric disorders

72
VPS16 core subunit of CORVET and HOPS complexes
DYT30, hVPS16
Autism, Dystonia, Metabolic syndrome, Peripheral neuropathy, Scoliosis, Diabetes mellitus type 2

73
VPS18 core subunit of CORVET and HOPS complexes
PEP3
Leukodystrophy

74
VPS26 retromer complex component A
HB58, Hbeta58, PEP8A, VPS26
Diabetes mellitus type 2, Diabetic retinopathy, Psoriasis

75
VPS26 endosomal protein sorting factor C
DCRA, DSCR3, DSCRA
Neurodevelopmental disorder, Oligodendroglioma, Diabetes mellitus type 2

76
VPS33A core subunit of CORVET and HOPS complexes
MPSPS
Desbuquois syndrome, Mucopolysaccharidosis

77
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

78
VPS35 retromer complex component
MEM3, PARK17
Parkinson disease, Ear, patella, short stature syndrome, Hereditary parkinson disease, Intellectual developmental disorder, Schizophrenia

79
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

80
Vacuolar protein sorting 36 homolog
C13orf9, CGI-145, EAP45
Lewy body disease