SNX4

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

Sorting nexin-4 is a protein that in humans is encoded by the SNX4 gene.[5][6]

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SNX4
Identifiers
AliasesSNX4, ATG24B, sorting nexin 4
External IDsOMIM: 605931; MGI: 1916400; HomoloGene: 36143; GeneCards: SNX4; OMA:SNX4 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003794

NM_080557

RefSeq (protein)

NP_003785

NP_542124

Location (UCSC)Chr 3: 125.45 – 125.52 MbChr 16: 33.07 – 33.12 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 associated with the long isoform of the leptin receptor and with receptor tyrosine kinases for platelet-derived growth factor, insulin, and epidermal growth factor in cell cultures, but its function is unknown. This protein may form oligomeric complexes with family members.[6]

Interactions

SNX4 has been shown to interact with BIN1.[7]

References

Further reading

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