WFS1
Wolfram syndrome 1 (wolframin)
别名:
WFRS, WFS, WFSL
物种:
Human WFS1 (7466), Mouse Wfs1 (22393), Rat Wfs1 (83725), dog WFS1 (482113), fruit fly wfs1 (42679), sheep WFS1 (101112732), cow WFS1 (100298456), domestic cat WFS1 (101092024), chicken WFS1 (422857), naked mole-rat Wfs1 (101711151)
UniProtKB ID:
基因ID:
- Human(7466) 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]
- Mouse(22393) Wolfram syndrome 1 homolog (human)
- Rat(83725) Wolfram syndrome 1 (wolframin)
- dog(482113) Wolfram syndrome 1 (wolframin)
- fruit fly(42679) wolfram syndrome 1
- sheep(101112732) Wolfram syndrome 1 (wolframin)
- cow(100298456) Wolfram syndrome 1 (wolframin)
- domestic cat(101092024) Wolfram syndrome 1 (wolframin)
- chicken(422857) Wolfram syndrome 1 (wolframin)
- naked mole-rat(101711151) Wolfram syndrome 1 (wolframin)
- domestic guinea pig(100731167) Wolfram syndrome 1 (wolframin)
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Antibodies
货号
说明
物种反应性
应用
Anti-WFS1 antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
物种反应性
human
应用
immunohistochemistry