Solute carrier family 16 member 12

Solute carrier family 16 member 12 is a protein that in humans is encoded by the SLC16A12 gene. [5]

SLC16A12
Identifiers
AliasesSLC16A12, CJMG, MCT12, CRT2, solute carrier family 16 member 12, CTRCT47
External IDsOMIM: 611910; MGI: 2147716; HomoloGene: 130007; GeneCards: SLC16A12; OMA:SLC16A12 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_213606

NM_172838

RefSeq (protein)

NP_998771

NP_766426

Location (UCSC)Chr 10: 89.43 – 89.56 MbChr 19: 34.65 – 34.72 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

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This gene encodes a transmembrane transporter that likely plays a role in monocarboxylic acid transport. A mutation in this gene has been associated with juvenile cataracts with microcornea and renal glucosuria. [provided by RefSeq, Mar 2010].

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000152779Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000009378Ensembl, 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 16 member 12". Retrieved 2018-10-06.

Further reading

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