SLC12A9

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SLC12A9
Identifiers
Aliases SLC12A9, CCC6, CIP1, WO3.3, hCCC6, solute carrier family 12 member 9
External IDs MGI: 1933532 HomoloGene: 5429 GeneCards: SLC12A9
Genetically Related Diseases
coronary artery disease[1]
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001267812
NM_001267814
NM_020246

NM_031406

RefSeq (protein)

NP_001254741
NP_001254743
NP_064631

NP_113583.2
NP_113583

Location (UCSC) Chr 7: 100.83 – 100.87 Mb Chr 5: 137.31 – 137.33 Mb
PubMed search [2] [3]
Wikidata
View/Edit Human View/Edit Mouse

Solute carrier family 12 member 9 (SLC12A9), also known as cation-chloride cotransporter 6 (CCC6) or cation-chloride cotransporter-interacting protein 1 (CIP1), is a protein that in humans is encoded by the SLC12A9 gene.[4][5][6]

References[edit]

  1. ^ "Diseases that are genetically associated with SLC12A9 view/edit references on wikidata". 
  2. ^ "Human PubMed Reference:". 
  3. ^ "Mouse PubMed Reference:". 
  4. ^ "Entrez Gene: solute carrier family 12 (potassium/chloride transporters)". 
  5. ^ Caron L; Rousseau F; Gagnon E; Isenring P (October 2000). "Cloning and functional characterization of a cation-Cl cotransporter-interacting protein". J. Biol. Chem. 275 (41): 32027–36. doi:10.1074/jbc.M000108200. PMID 10871601. 
  6. ^ Wilson MD; Riemer C; Martindale DW; Schnupf P; Boright AP; Cheung TL; Hardy DM; Schwartz S; Scherer SW; Tsui LC; Miller W; Koop BF (March 2001). "Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5". Nucleic Acids Res. 29 (6): 1352–65. doi:10.1093/nar/29.6.1352. PMC 29746Freely accessible. PMID 11239002. 

Further reading[edit]