Solute carrier family 38 member 9

Last updated
SLC38A9
Identifiers
Aliases SLC38A9 , URLC11, solute carrier family 38 member 9
External IDs OMIM: 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 Mb Chr 13: 112.8 – 112.88 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

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


References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000177058 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000047789 Ensembl, May 2017
  3. '"`UNIQ--templatestyles-00000006-QINU`"' "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. '"`UNIQ--templatestyles-00000008-QINU`"' "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