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Protein-coding gene in the species Homo sapiens

SNX4

SNX4
All data from the card 17
Aliases
SNX4, ATG24B, sorting nexin 4
External IDs
OMIM: 605931; MGI: 1916400; GeneCards: SNX4
Chr.
Chromosome 3 (human)
Band
3q21.2
End
125,520,202 bp
Chr.
Chromosome 16 (mouse)
Band
16|16 B3
End
33,120,639 bp
BioGPS
More reference expression data
Databases
NCBI: entry; OMA: entry
Species
Human
Entrez
8723
Ensembl
ENSG00000114520
UniProt
O95219
RefSeq (mRNA)
NM_003794
RefSeq (protein)
NP_003785
Location (UCSC)
Chr 3: 125.45 – 125.52 Mb

Sorting nexin-4 is a protein that in humans is encoded by the SNX4 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 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.

Interactions

SNX4 has been shown to interact with BIN1.

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