SNX27

Sorting nexin family member 27
Available structures
PDB Ortholog search: PDBe, RCSB
Identifiers
Symbols SNX27 ; MRT1; MY014
External IDs OMIM: 611541 MGI: 1923992 HomoloGene: 12797 GeneCards: SNX27 Gene
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez 81609 76742
Ensembl ENSG00000143376 ENSMUSG00000028136
UniProt Q96L92 Q3UHD6
RefSeq (mRNA) NM_030918 NM_001082484
RefSeq (protein) NP_112180 NP_001075953
Location (UCSC) Chr 1:
151.61 – 151.7 Mb
Chr 3:
94.5 – 94.58 Mb
PubMed search

Sorting nexin family member 27, also known as SNX27, is a human gene.[1]

This gene encodes a member of the sorting nexin family, a diverse group of cytoplasmic and membrane-associated proteins involved in endocytosis of plasma membrane receptors and protein trafficking through these compartments. All members of this protein family contain a phosphoinositide binding domain (PX domain). A highly similar protein in mice is responsible for the specific recruitment of an isoform of the serotonin 5-hydroxytryptamine 4 receptor into early endosomes, suggesting the analogous role for the human protein.[1] "Loss of sorting nexin 27 contributes to excitatory synaptic dysfunction by modulating glutamate receptor recycling in Down's syndrome" by Xin Wang et al. was published in Nature Medicine on March 24, 2013.

References

Further reading

This article is issued from Wikipedia - version of the Monday, July 27, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.