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Protein-coding gene in the species Homo sapiens

SNX9

SNX9
All data from the card 18
Aliases
SNX9, SDP1, SH3PX1, SH3PXD3A, WISP, sorting nexin 9
External IDs
OMIM: 605952; MGI: 1913866; GeneCards: SNX9
PDB
Ortholog search: PDBe RCSB
Chr.
Chromosome 6 (human)
Band
6q25.3
End
157,945,077 bp
Chr.
Chromosome 17 (mouse)
Band
17 A1|17 3.51 cM
End
5,982,229 bp
BioGPS
More reference expression data
Databases
NCBI: entry; OMA: entry
Species
Human
Entrez
51429
Ensembl
ENSG00000130340
UniProt
Q9Y5X1
RefSeq (mRNA)
NM_016224
RefSeq (protein)
NP_057308
Location (UCSC)
Chr 6: 157.7 – 157.95 Mb

Sorting nexin-9 is a protein that in humans is encoded by the SNX9 gene.

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.

Interactions

SNX9 has been shown to interact with ADAM9, DNM2 and ADAM15.

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Text from Wikipedia, CC BY-SA 4.0 · Source article