SNX21 sorting nexin family member 21 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 90203)
Symbol: SNX21
Full name: sorting nexin family member 21
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: C20orf161; PP3993; SNX-L; SNXL; dJ337O18.4
Summary: This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members. The specific function of this protein has not been determined. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
Expression: Ubiquitous expression in skin (RPKM 12.2), fat (RPKM 8.5) and 24 other tissues
Orthologs: mouse
Gene size: 9478bp
Exon count: 7