SNX13 sorting nexin 13 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 23161)
Symbol: SNX13
Full name: sorting nexin 13
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: RGS-PX1
Summary: This gene encodes a PHOX domain- and RGS domain-containing protein that belongs to the sorting nexin (SNX) family and the regulator of G protein signaling (RGS) family. The PHOX domain is a phosphoinositide binding domain, and the SNX family members are involved in intracellular trafficking. The RGS family members are regulatory molecules that act as GTPase activating proteins for G alpha subunits of heterotrimeric G proteins. The RGS domain of this protein interacts with G alpha(s), accelerates its GTP hydrolysis, and attenuates G alpha(s)-mediated signaling. Overexpression of this protein delayes lysosomal degradation of the epidermal growth factor receptor. Because of its bifunctional role, this protein may link heterotrimeric G protein signaling and vesicular trafficking. [provided by RefSeq, Jul 2008]
Expression: Ubiquitous expression in thyroid (RPKM 8.8), testis (RPKM 6.4) and 25 other tissues
Orthologs: mouse
Gene size: 149734bp
Exon count: 31