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SNX5

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Protein-coding gene in the species Homo sapiens
SNX5
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

1SYS

Identifiers
AliasesSNX5, sorting nexin 5
External IDsOMIM: 605937; MGI: 1916428; HomoloGene: 40944; GeneCards: SNX5; OMA:SNX5 - orthologs
Gene location (Human)
Chromosome 20 (human)
Chr.Chromosome 20 (human)
Chromosome 20 (human)Genomic location for SNX5Genomic location for SNX5
Band20p11.23Start17,941,597 bp
End17,968,980 bp
Gene location (Mouse)
Chromosome 2 (mouse)
Chr.Chromosome 2 (mouse)
Chromosome 2 (mouse)Genomic location for SNX5Genomic location for SNX5
Band2 G1|2 70.98 cMStart144,092,043 bp
End144,112,826 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • left lobe of thyroid gland

  • right lobe of thyroid gland

  • ventricular zone

  • Achilles tendon

  • rectum

  • gonad

  • spleen

  • corpus epididymis

  • secondary oocyte

  • left ovary
Top expressed in
  • stroma of bone marrow

  • tail of embryo

  • abdominal wall

  • epiblast

  • Gonadal ridge

  • mandibular prominence

  • dermis

  • efferent ductule

  • migratory enteric neural crest cell

  • maxillary prominence
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

27131

69178

Ensembl

ENSG00000089006

ENSMUSG00000027423

UniProt

Q9Y5X3
Q5QPE4

Q9D8U8

RefSeq (mRNA)

NM_152227
NM_001282454
NM_014426

NM_001199188
NM_024225

RefSeq (protein)

NP_001269383
NP_055241
NP_689413

NP_001186117
NP_077187

Location (UCSC)Chr 20: 17.94 – 17.97 MbChr 2: 144.09 – 144.11 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Sorting nexin-5 is a protein that in humans is encoded by the SNX5 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 is a component of the mammalian retromer complex, which facilitates cargo retrieval from endosomes to the trans-Golgi network. It has also been shown to bind to the Fanconi anemia, complementation group A protein. This gene results in two transcript variants encoding the same protein.

Interactions

SNX5 has been shown to interact with FANCA.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000089006Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000027423Ensembl, 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. ^ Otsuki T; Kajigaya S; Ozawa K; Liu JM (Jan 2000). "SNX5, a new member of the sorting nexin family, binds to the Fanconi anemia complementation group A protein". Biochem Biophys Res Commun. 265 (3): 630–5. doi:10.1006/bbrc.1999.1731. PMID 10600472.
  6. ^ Wassmer T; Attar N; Bujny MV; Oakley J; Traer CJ; Cullen PJ (Dec 2006). "A loss-of-function screen reveals SNX5 and SNX6 as potential components of the mammalian retromer". J Cell Sci. 120 (Pt 1): 45–54. doi:10.1242/jcs.03302. PMID 17148574.
  7. ^ "Entrez Gene: SNX5 sorting nexin 5".

Further reading


Sorting nexins
SNX-BAR
SNX-PX
SNX-Other
Related articles


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