Motile sperm domain containing 2

MOSPD2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMOSPD2, Motile sperm domain containing 2
External IDsMGI: 1924013 HomoloGene: 22125 GeneCards: MOSPD2
Gene location (Human)
Chr.X chromosome (human)[1]
BandXp22.2Start14,873,441 bp[1]
End14,922,327 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

158747

76763

Ensembl

ENSG00000130150

ENSMUSG00000061778

UniProt

Q8NHP6

Q9CWP6

RefSeq (mRNA)

NM_001177475
NM_152581
NM_001330241

NM_001290523
NM_001290524
NM_029730

RefSeq (protein)

NP_001170946
NP_001317170
NP_689794

NP_001277452
NP_001277453
NP_084006

Location (UCSC)Chr X: 14.87 – 14.92 MbChr X: 164.94 – 164.98 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Motile sperm domain containing 2 is a protein that in humans is encoded by the MOSPD2 gene.[5] It is an endoplasmic reticulum–resident protein involved in membrane contact site formation.[6]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000130150 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000061778 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:".
  4. ↑ "Mouse PubMed Reference:".
  5. ↑ "Entrez Gene: Motile sperm domain containing 2".
  6. ↑ Di Mattia T, Wilhelm LP, Ikhlef S, Wendling C, Spehner D, Nominé Y, Giordano F, Mathelin C, Drin G, Tomasetto C, Alpy F (June 2018). "Identification of MOSPD2, a novel scaffold for endoplasmic reticulum membrane contact sites". EMBO Reports. 19 (7): e45453. doi:10.15252/embr.201745453. PMC 6030701. PMID 29858488.

Further reading

  • Velez Edwards DR, Naj AC, Monda K, North KE, Neuhouser M, Magvanjav O, Kusimo I, Vitolins MZ, Manson JE, O'Sullivan MJ, Rampersaud E, Edwards TL (March 2013). "Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study". Human Genetics. 132 (3): 323–36. doi:10.1007/s00439-012-1246-3. PMC 3704217. PMID 23192594.
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