SLC4A11

From Wikipedia, the free encyclopedia
Jump to: navigation, search
SLC4A11
Identifiers
Aliases SLC4A11, BTR1, CDPD1, CHED2, NABC1, dJ794I6.2, CHED, solute carrier family 4 member 11
External IDs MGI: 2138987 HomoloGene: 12931 GeneCards: 83959
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001174089
NM_001174090
NM_032034

NM_001081162

RefSeq (protein)

NP_001167560.1
NP_001167561.1
NP_114423.1

NP_001074631.1

Location (UCSC) Chr 20: 3.23 – 3.24 Mb Chr 2: 130.68 – 130.7 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

Sodium bicarbonate transporter-like protein 11 is a protein that in humans is encoded by the SLC4A11 gene.[1][2][3][4]

See also[edit]

References[edit]

  1. ^ Luong A, Hannah VC, Brown MS, Goldstein JL (Sep 2000). "Molecular characterization of human acetyl-CoA synthetase, an enzyme regulated by sterol regulatory element-binding proteins". J Biol Chem 275 (34): 26458–66. doi:10.1074/jbc.M004160200. PMID 10843999. 
  2. ^ Parker MD, Ourmozdi EP, Tanner MJ (Apr 2001). "Human BTR1, a new bicarbonate transporter superfamily member and human AE4 from kidney". Biochem Biophys Res Commun 282 (5): 1103–9. doi:10.1006/bbrc.2001.4692. PMID 11302728. 
  3. ^ Vithana EN, Morgan P, Sundaresan P, Ebenezer ND, Tan DT, Mohamed MD, Anand S, Khine KO, Venkataraman D, Yong VH, Salto-Tellez M, Venkatraman A, Guo K, Hemadevi B, Srinivasan M, Prajna V, Khine M, Casey JR, Inglehearn CF, Aung T (Jun 2006). "Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)". Nat Genet 38 (7): 755–7. doi:10.1038/ng1824. PMID 16767101. 
  4. ^ "Entrez Gene: SLC4A11 solute carrier family 4, sodium bicarbonate transporter-like, member 11". 

Further reading[edit]