SNX27

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SNX27
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesSNX27, MRT1, MY014, sorting nexin family member 27, sorting nexin 27
External IDsOMIM: 611541; MGI: 1923992; HomoloGene: 12797; GeneCards: SNX27; OMA:SNX27 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_030918
NM_001330723

NM_001082484
NM_029721

RefSeq (protein)

NP_001317652
NP_112180

NP_001075953
NP_083997

Location (UCSC)Chr 1: 151.61 – 151.7 MbChr 3: 94.4 – 94.49 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Sorting nexin family member 27, also known as SNX27, is a human gene.[5]

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.[5] "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. [1]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000143376Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028136Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "Entrez Gene: SNX27 sorting nexin family member 27".

Further reading

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