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SLC4A11

Official Full Name
solute carrier family 4 member 11
Organism
Homo sapiens
GeneID
83959
Background
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]
Synonyms
BTR1; CHED; CDPD1; CHED2; NABC1; dJ794I6.2;

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