RecName: Full=Sorting nexin-15

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A clinical, genetic and candidate gene study of Silver syndrome, a complicated form of hereditary spastic paraplegia. [J Neurol. 2004]
A clinical, genetic and candidate gene study of Silver syndrome, a complicated form of hereditary spastic paraplegia.
Warner TT, Patel H, Proukakis C, Reed JA, McKie L, Wills A, Patton MA, Crosby AH. J Neurol. 2004 Sep; 251(9):1068-74.
Overexpression of a novel sorting nexin, SNX15, affects endosome morphology and protein trafficking. [Traffic. 2000]
Overexpression of a novel sorting nexin, SNX15, affects endosome morphology and protein trafficking.
Barr VA, Phillips SA, Taylor SI, Haft CR. Traffic. 2000 Nov; 1(11):904-16.
SNX15 links clathrin endocytosis to the PtdIns3P early endosome independently of the APPL1 endosome. [J Cell Sci. 2013]
SNX15 links clathrin endocytosis to the PtdIns3P early endosome independently of the APPL1 endosome.
Danson C, Brown E, Hemmings OJ, McGough IJ, Yarwood S, Heesom KJ, Carlton JG, Martin-Serrano J, May MT, Verkade P, et al. J Cell Sci. 2013 Nov 1; 126(Pt 21):4885-99. Epub 2013 Aug 28.

RefSeq genomic sequence
See the genomic reference sequence for the SNX15 gene (NG_029947.2).
RefSeq protein isoforms
See 2 reference sequence protein isoforms for the SNX15 gene.

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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein