SLC12A3 FISH Probe

This gene encodes a renal thiazide-sensitive sodium-chloride cotransporter that is important for electrolyte homeostasis. This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. Mutations in this gene cause Gitelman syndrome, a disease similar to Bartter's syndrome, that is characterized by hypokalemic alkalosis combined with hypomagnesemia, low urinary calcium, and increased renin activity associated with normal blood pressure. This cotransporter is the target for thiazide diuretics that are used for treating high blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
SLC12A3-20-RE 20 (40 μL) 200 μL color Request Pricing
SLC12A3-20-OR 20 (40 μL) 200 μL color Request Pricing
SLC12A3-20-GO 20 (40 μL) 200 μL color Request Pricing
SLC12A3-20-GR 20 (40 μL) 200 μL color Request Pricing
SLC12A3-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene Summary

This gene encodes a renal thiazide-sensitive sodium-chloride cotransporter that is important for electrolyte homeostasis. This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. Mutations in this gene cause Gitelman syndrome, a disease similar to Bartter's syndrome, that is characterized by hypokalemic alkalosis combined with hypomagnesemia, low urinary calcium, and increased renin activity associated with normal blood pressure. This cotransporter is the target for thiazide diuretics that are used for treating high blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Gene Details

Gene Symbol : SLC12A3

Gene Name : Solute carrier family 12 member 3

Chromosome : CHR 16: 568,652,06-569,158,49

Locus : 16q13

Alt. Genes : PREB

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