SLC4A11

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Solute carrier family 4, sodium borate transporter, member 11
Identifiers
Symbols SLC4A11 ; BTR1; CDPD1; CHED2; NABC1; dJ794I6.2
External IDs OMIM610206 MGI2138987 HomoloGene12931 GeneCards: SLC4A11 Gene
Orthologs
Species Human Mouse
Entrez 83959 269356
Ensembl ENSG00000088836 ENSMUSG00000074796
UniProt Q8NBS3 A2AJN7
RefSeq (mRNA) NM_001174089 NM_001081162
RefSeq (protein) NP_001167560 NP_001074631
Location (UCSC) Chr 20:
3.21 – 3.22 Mb
Chr 2:
130.68 – 130.7 Mb
PubMed search [1] [2]

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]