Solute carrier family 38 member 9

Solute carrier family 38 member 9 is a protein that in humans is encoded by the SLC38A9 gene. [5]

SLC38A9
Identifiers
AliasesSLC38A9, URLC11, solute carrier family 38 member 9
External IDsOMIM: 616203 MGI: 1918839 HomoloGene: 18139 GeneCards: SLC38A9
Gene location (Human)
Chr.Chromosome 5 (human)[1]
Band5q11.2Start55,625,845 bp[1]
End55,773,194 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

153129

268706

Ensembl

ENSG00000177058

ENSMUSG00000047789

UniProt

Q8NBW4

Q8BGD6

RefSeq (mRNA)

NM_175376
NM_178746

RefSeq (protein)

NP_848861

Location (UCSC)Chr 5: 55.63 – 55.77 MbChr 13: 112.66 – 112.74 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse


References

  1. GRCh38: Ensembl release 89: ENSG00000177058 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000047789 - Ensembl, 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. "Entrez Gene: Solute carrier family 38 member 9". Retrieved 2018-08-06.

Further reading


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