SNX17

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Sorting nexin-17 is a protein that in humans is encoded by the SNX17 gene.[5][6][7]

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SNX17
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesSNX17, sorting nexin 17
External IDsOMIM: 605963; MGI: 2387801; HomoloGene: 8838; GeneCards: SNX17; OMA:SNX17 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001267059
NM_001267060
NM_001267061
NM_014748

NM_153680

RefSeq (protein)

NP_001253988
NP_001253989
NP_001253990
NP_055563

NP_710147

Location (UCSC)Chr 2: 27.37 – 27.38 MbChr 5: 31.35 – 31.36 Mb
PubMed search[3][4]
Wikidata
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Function

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, but contains a B41 domain. This protein interacts with the cytoplasmic domain of P-selectin, and may function in the intracellular trafficking of P-selectin.[7]

Interactions

References

Further reading

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