Solute carrier family 41, member 3 is a protein that in humans is encoded by the SLC41A3 gene.[5]

SLC41A3
Identifiers
AliasesSLC41A3, SLC41A1-L2, solute carrier family 41 member 3
External IDsOMIM: 610803; MGI: 1918949; HomoloGene: 23052; GeneCards: SLC41A3; OMA:SLC41A3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001008485
NM_001008486
NM_001008487
NM_001164475
NM_017836

NM_001037493
NM_027868

RefSeq (protein)

NP_001032570
NP_082144

Location (UCSC)Chr 3: 126.01 – 126.1 MbChr 6: 90.58 – 90.62 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

References

edit
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000114544Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000030089Ensembl, 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 41, member 3". Retrieved 2011-09-28.

Further reading

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  • Wabakken T, Rian E, Kveine M, Aasheim HC (July 2003). "The human solute carrier SLC41A1 belongs to a novel eukaryotic subfamily with homology to prokaryotic MgtE Mg2+ transporters". Biochemical and Biophysical Research Communications. 306 (3): 718–24. doi:10.1016/S0006-291X(03)01030-1. PMID 12810078.