SLC46A3

Solute carrier family 46, member 3 is a protein that in humans is encoded by the SLC46A3 gene.[5]

SLC46A3
Identifiers
AliasesSLC46A3, FKSG16, SLC46A3 (gene), solute carrier family 46 member 3
External IDsOMIM: 616764 MGI: 1918956 HomoloGene: 41733 GeneCards: SLC46A3
Gene location (Human)
Chr.Chromosome 13 (human)[1]
Band13q12.3Start28,700,064 bp[1]
End28,718,970 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

283537

71706

Ensembl

ENSG00000139508

ENSMUSG00000029650

UniProt

Q7Z3Q1

Q9DC26

RefSeq (mRNA)

NM_001135919
NM_181785
NM_001347960

NM_027872
NM_001357002

RefSeq (protein)

NP_001129391
NP_861450
NP_001334889

NP_082148
NP_001343931

Location (UCSC)Chr 13: 28.7 – 28.72 MbChr 5: 147.88 – 147.89 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

References

  1. GRCh38: Ensembl release 89: ENSG00000139508 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000029650 - 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 46, member 3".

Further reading


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