SLC22A14

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SLC22A14
Identifiers
AliasesSLC22A14, OCTL2, OCTL4, ORCTL4, solute carrier family 22 member 14
External IDsOMIM: 604048 MGI: 2685974 HomoloGene: 3530 GeneCards: SLC22A14
Gene location (Human)
Chromosome 3 (human)
Chr.Chromosome 3 (human)[1]
Chromosome 3 (human)
Genomic location for SLC22A14
Genomic location for SLC22A14
Band3p22.2Start38,282,294 bp[1]
End38,318,575 bp[1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004803
NM_001320033

NM_001037749

RefSeq (protein)

NP_001306962
NP_004794

n/a

Location (UCSC)Chr 3: 38.28 – 38.32 MbChr 9: 119.17 – 119.37 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Solute carrier family 22 member 14 is a protein that in humans is encoded by the SLC22A14 gene.[5]

Function[edit]

This gene encodes a member of the organic-cation transporter family. It is located in a gene cluster with another member of the family, organic cation transporter like 3. The encoded protein is a transmembrane protein which is thought to transport small molecules and since this protein is conserved among several species, it is suggested to have a fundamental role in mammalian systems. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016].

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000144671 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000070280 - 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 22 member 14". Retrieved 2020-01-19.

Further reading[edit]

This article incorporates text from the United States National Library of Medicine, which is in the public domain.