SLC22A14

Mammalian protein found in Homo sapiens From Wikipedia, the free encyclopedia

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

AliasesSLC22A14, OCTL2, OCTL4, ORCTL4, solute carrier family 22 member 14
End38,318,575 bp[1]
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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; OMA:SLC22A14 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004803
NM_001320033

NM_001037749

RefSeq (protein)

NP_001306962
NP_004794

NP_001032838

Location (UCSC)Chr 3: 38.28 – 38.32 MbChr 9: 119 – 119.19 Mb
PubMed search[3][4]
Wikidata
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Function

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

Further reading

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