SNX15

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

Sorting nexin-15 is a protein that in humans is encoded by the SNX15 gene.[4][5]

AliasesSNX15, HSAF001435, sorting nexin 15
Chr.Chromosome 19 (mouse)[1]
End6,178,334 bp[1]
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SNX15
Identifiers
AliasesSNX15, HSAF001435, sorting nexin 15
External IDsOMIM: 605964; MGI: 1916274; HomoloGene: 12294; GeneCards: SNX15; OMA:SNX15 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_147777
NM_013306

NM_026912

RefSeq (protein)

NP_037438
NP_680086

NP_081188

Location (UCSC)n/aChr 19: 6.17 – 6.18 Mb
PubMed search[2][3]
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. Overexpression of this gene results in a decrease in the processing of insulin and hepatocyte growth factor receptors to their mature subunits. This decrease is caused by the mislocalization of furin, the endoprotease responsible for cleavage of insulin and hepatocyte growth factor receptors. This protein is involved in endosomal trafficking from the plasma membranee to recycling endosomes or the trans-Golgi network. This gene encodes two transcript variants encoding distinct isoforms.[5]

References

Further reading

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