VPS13B vacuolar protein sorting 13 homolog B [ Homo sapiens (human) ]
Source: NCBI Gene (ID 157680)
Symbol: VPS13B
Full name: vacuolar protein sorting 13 homolog B
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: BLTP5B; CHS1; COH1
Summary: This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
Expression: Ubiquitous expression in endometrium (RPKM 3.0), ovary (RPKM 2.8) and 25 other tissues
Orthologs: mouse
Gene size: 864307bp
Exon count: 65