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
14661 to 14670 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14661
Vacuolar protein sorting 13 homolog C
BLTP5C, PARK23
Parkinson disease, Bipolar disorder, Diabetic retinopathy, Hemiparkinsonism, Major depressive disorder, Metabolic syndrome, Oligodendroglioma, Alzheimer disease, Schizophrenia, Thyroid hemiagenesis, Diabetes mellitus type 2

14662
Vacuolar protein sorting 13 homolog D
BLTP5D, SCA24, SCAR4, SCASI
Arthrogryposis multiplex congenita, Spinocerebellar ataxia, Atrophic gastritis, Cerebellar ataxia, Central nervous system cancer, Cholecystolithiasis, Glioblastoma, Glioma, Non-immune hydrops fetalis, Leigh syndrome, Neurodevelopmental disorder, Pena-shokeir syndrome , Psychiatric disorders

14663
VPS16 core subunit of CORVET and HOPS complexes
DYT30, hVPS16
Autism, Dystonia, Metabolic syndrome, Peripheral neuropathy, Scoliosis, Diabetes mellitus type 2

14664
VPS18 core subunit of CORVET and HOPS complexes
PEP3
Leukodystrophy

14665
VPS26 retromer complex component A
HB58, Hbeta58, PEP8A, VPS26
Diabetes mellitus type 2, Diabetic retinopathy, Psoriasis

14666
VPS26 endosomal protein sorting factor C
DCRA, DSCR3, DSCRA
Neurodevelopmental disorder, Oligodendroglioma, Diabetes mellitus type 2

14667
VPS33A core subunit of CORVET and HOPS complexes
MPSPS
Desbuquois syndrome, Mucopolysaccharidosis

14668
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

14669
VPS35 retromer complex component
MEM3, PARK17
Parkinson disease, Ear, patella, short stature syndrome, Hereditary parkinson disease, Intellectual developmental disorder, Schizophrenia

14670
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