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SLC4A11 产品

(Solute Carrier Family 4, Sodium Borate Transporter, Member 11 (SLC4A11))

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This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010].

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Featured SLC4A11 Categories

SLC4A11 抗体

High quality antibodies with extensive validation data.

SLC4A11 蛋白

Proteins for various applications incl. WB, ELISA, IF etc.

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Latest Publications for our SLC4A11 Products

Vithana, Morgan, Ramprasad, Tan, Yong, Venkataraman, Venkatraman, Yam, Nagasamy, Law, Rajagopal, Pang, Kumaramanickevel, Casey, Aung: "SLC4A11 mutations in Fuchs endothelial corneal dystrophy." in: Human molecular genetics, Vol. 17, Issue 5, pp. 656-66, (2008) (PubMed).

Hemadevi, Veitia, Srinivasan, Arunkumar, Prajna, Lesaffre, Sundaresan: "Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy." in: Archives of ophthalmology (Chicago, Ill. : 1960), Vol. 126, Issue 5, pp. 700-8, (2008) (PubMed).

Jiao, Sultana, Garg, Ramamurthy, Vemuganti, Gangopadhyay, Hejtmancik, Kannabiran: "Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11." in: Journal of medical genetics, Vol. 44, Issue 1, pp. 64-8, (2007) (PubMed).

Desir, Moya, Reish, Van Regemorter, Deconinck, David, Meire, Abramowicz: "Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy." in: Journal of medical genetics, Vol. 44, Issue 5, pp. 322-6, (2007) (PubMed).

Vithana, Morgan, Sundaresan, Ebenezer, Tan, Mohamed, Anand, Khine, Venkataraman, Yong, Salto-Tellez, Venkatraman, Guo, Hemadevi, Srinivasan, Prajna, Khine, Casey, Inglehearn, Aung: "Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)." in: Nature genetics, Vol. 38, Issue 7, pp. 755-7, (2006) (PubMed).

Park, Li, Shcheynikov, Zeng, Muallem: "NaBC1 is a ubiquitous electrogenic Na+ -coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation." in: Molecular cell, Vol. 16, Issue 3, pp. 331-41, (2004) (PubMed).

Parker, Ourmozdi, Tanner: "Human BTR1, a new bicarbonate transporter superfamily member and human AE4 from kidney." in: Biochemical and biophysical research communications, Vol. 282, Issue 5, pp. 1103-9, (2001) (PubMed).

Synonyms and alternative names related to SLC4A11

solute carrier family 4 member 11 (Slc4a11), solute carrier family 4 member 11 (SLC4A11), solute carrier family 4 member 11 L homeolog (slc4a11.L), solute carrier family 4 member 11 (slc4a11), solute carrier family 4, sodium borate transporter, member 11 (slc4a11), solute carrier family 4, sodium bicarbonate transporter-like, member 11 (Slc4a11), AI503023, BTR1, CDPD1, CHED2, dJ794I6.2, NaBC1, NABC1, si:dkey-12j14.4

Protein level used designations for SLC4A11

  • sodium bicarbonate transporter-like protein 11
  • solute carrier family 4, sodium bicarbonate transporter-like, member 11
  • solute carrier family 4, sodium borate transporter, member 11
  • sodium-coupled borate transporter
  • sodium bicarbonate transporter-like protein 11-like
  • solute carrier family 4 member 11
  • Sodium borate cotransporter 1
  • Solute carrier family 4 member 11
  • bicarbonate transporter-related protein 1
  • bicarbonate transporter related protein 1
  • sodium-coupled borate cotransporter 1
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