SNX13

Gene of the species Homo sapiens From Wikipedia, the free encyclopedia

Sorting nexin-13 is a protein that in humans is encoded by the SNX13 gene.[4][5][6]

AliasesSNX13, RGS-PX1, sorting nexin 13
Chr.Chromosome 12 (mouse)[1]
End35,197,478 bp[1]
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Function

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 delays lysosomal degradation of the epidermal growth factor receptor. Because of its bifunctional role, this protein may link heterotrimeric G protein signaling and vesicular trafficking.[6]

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