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; OMA:SLC38A9 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_175376
NM_178746

RefSeq (protein)

NP_848861

Location (UCSC)Chr 5: 55.63 – 55.77 MbChr 13: 112.8 – 112.88 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse


References

edit
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000177058Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000047789Ensembl, 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

edit