SLC23A2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

SLC23A2

Solute carrier family 23 member 2 is a protein that in humans is encoded by the SLC23A2 gene.[5][6][7]

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SLC23A2
Identifiers
AliasesSLC23A2, NBTL1, SLC23A1, SVCT2, YSPL2, hSVCT2, solute carrier family 23 member 2
External IDsOMIM: 603791; MGI: 1859682; HomoloGene: 68440; GeneCards: SLC23A2; OMA:SLC23A2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005116
NM_203327

NM_018824
NM_001355430
NM_001355431

RefSeq (protein)

NP_005107
NP_976072

NP_061294
NP_001342359
NP_001342360

Location (UCSC)Chr 20: 4.85 – 5.01 MbChr 2: 131.89 – 131.99 Mb
PubMed search[3][4]
Wikidata
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The absorption of vitamin C into the body and its distribution to organs requires two sodium-dependent vitamin C transporters. This gene encodes one of the two required transporters and the encoded protein accounts for tissue-specific uptake of vitamin C. Previously, this gene had an official symbol of SLC23A1.[7]

See also

References

Further reading

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