SNX9

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

Sorting nexin-9 is a protein that in humans is encoded by the SNX9 gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesSNX9, SDP1, SH3PX1, SH3PXD3A, WISP, sorting nexin 9
Quick facts Available structures, PDB ...
SNX9
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesSNX9, SDP1, SH3PX1, SH3PXD3A, WISP, sorting nexin 9
External IDsOMIM: 605952; MGI: 1913866; HomoloGene: 49454; GeneCards: SNX9; OMA:SNX9 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_016224

NM_025664

RefSeq (protein)

NP_057308

NP_079940

Location (UCSC)Chr 6: 157.7 – 157.95 MbChr 17: 5.89 – 5.98 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 does contain an SH3 domain near its N-terminus. This protein interacts with the cytoplasmic domains of the precursor but not the processed forms of a disintegrin and metalloprotease domain 9 and 15. This protein binds the beta-appendage domain of adaptor protein 2 and may function to assist adaptor protein 2 in its role at the plasma membrane. This protein interacts with activated Cdc42-associated kinase-2 to regulate the degradation of epidermal growth factor receptor protein.[7]

Interactions

SNX9 has been shown to interact with ADAM9,[5] DNM2[8] and ADAM15.[5]

References

Further reading

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