Your search for "slc4a11" returned 180 TaqMan® SNP Genotyping Assays
solute carrier family 4 member 11
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]
AI503023, BTR1, CDPD1, CHED, CHED2, DJ794I6.2, NABC1, SLC4A11
Please enter the information below and press OK to send your cart to Core Services for purchase.