Solute carrier family 12 member 8 (SLC12A8), also known as cation-chloride cotransporter 9 (CCC9), is a protein that in humans is encoded by the SLC12A8 gene.[5][6]

SLC12A8
Identifiers
AliasesSLC12A8, CCC9, solute carrier family 12 member 8
External IDsOMIM: 611316; MGI: 2443672; HomoloGene: 11628; GeneCards: SLC12A8; OMA:SLC12A8 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_024628
NM_001195483

NM_001083902
NM_134251
NM_001370999

RefSeq (protein)

NP_001182412
NP_078904

NP_001077371
NP_599012
NP_001357928

Location (UCSC)Chr 3: 125.08 – 125.21 MbChr 16: 33.34 – 33.48 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000221955Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000035506Ensembl, 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 12 (potassium/chloride transporters)".
  6. ^ Hewett D, Samuelsson L, Polding J, Enlund F, Smart D, Cantone K, See CG, Chadha S, Inerot A, Enerback C, Montgomery D, Christodolou C, Robinson P, Matthews P, Plumpton M, Wahlstrom J, Swanbeck G, Martinsson T, Roses A, Riley J, Purvis I (March 2002). "Identification of a psoriasis susceptibility candidate gene by linkage disequilibrium mapping with a localized single nucleotide polymorphism map". Genomics. 79 (3): 305–14. doi:10.1006/geno.2002.6720. PMID 11863360.

Further reading

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