SNAG1

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

Sorting nexin-18 is a protein that in humans is encoded by the SNX18 gene.[5][6][7]

AliasesSNX18, SH3PX2, SH3PXD3B, SNAG1, sorting nexin 18
End54,546,586 bp[1]
Quick facts SNX18, Identifiers ...
SNX18
Identifiers
AliasesSNX18, SH3PX2, SH3PXD3B, SNAG1, sorting nexin 18
External IDsMGI: 2137642; HomoloGene: 14164; GeneCards: SNX18; OMA:SNX18 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_052870
NM_001102575
NM_001145427

NM_130796

RefSeq (protein)

NP_001096045
NP_001138899
NP_443102

NP_570614

Location (UCSC)Chr 5: 54.52 – 54.55 MbChr 13: 113.73 – 113.76 Mb
PubMed search[3][4]
Wikidata
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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 SH3 domain. The specific function of this protein has not been determined.[7]

References

Further reading

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