WFS1 FISH Probe

This gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta-cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system. Mutations in this gene can also cause autosomal dominant deafness 6 (DFNA6), also known as DFNA14 or DFNA38. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2009]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
WFS1-20-RE 20 (40 μL) 200 μL color Request Pricing
WFS1-20-OR 20 (40 μL) 200 μL color Request Pricing
WFS1-20-GO 20 (40 μL) 200 μL color Request Pricing
WFS1-20-GR 20 (40 μL) 200 μL color Request Pricing
WFS1-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene Summary

This gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta-cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system. Mutations in this gene can also cause autosomal dominant deafness 6 (DFNA6), also known as DFNA14 or DFNA38. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2009]

Gene Details

Gene Symbol : WFS1

Gene Name : Wolframin ER transmembrane glycoprotein

Chromosome : CHR 4: 626,036,7-630,326,4

Locus : 4p16.1

Alt. Genes : HIPK3

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