WFS1

gene product
DFNA14, DFNA38, DFNA6, DIDMOAD, WFS
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]
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Antibodypedia Validation Initiative

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169 antibodies from 24 providers.

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Antibody
Proteintech Group
3 antibodies
NovoPro Bioscience Inc.
2 antibodies
Abnova Corporation
2 antibodies
LifeSpan BioSciences, Inc.
14 antibodies
antibodies-online
56 antibodies
Affinity Biosciences
1 antibody
Bioworld Technology, Inc
3 antibodies
Invitrogen Antibodies
3 antibodies
Abbkine Scientific Co.Ltd.
1 antibody
Cell Signaling Technology, Inc
1 antibody
Biorbyt
11 antibodies
Novus Biologicals
2 antibodies
GeneTex
2 antibodies
Atlas Antibodies
1 antibody
R&D Systems
1 antibody
Creative Biolabs
3 antibodies
St John's Laboratory
2 antibodies
United States Biological
36 antibodies
Creative Diagnostics
4 antibodies
MyBioSource
2 antibodies
Leading Biology
1 antibody
Sigma-Aldrich
1 antibody
Abbexa
2 antibodies