WFS1 抗体
(Wolfram Syndrome 1 (WFS1))
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].
Recommended next Filters:
您想试用我们的人工智能搜索吗？
52 results
Latest Publications for our WFS1 抗体
: "WFS1 is a novel component of the unfolded protein response and maintains homeostasis of the endoplasmic reticulum in pancreatic beta-cells." in: The Journal of biological chemistry, Vol. 280, Issue 47, pp. 39609-15, (2005) (PubMed).: "WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain." in: Human molecular genetics, Vol. 10, Issue 5, pp. 477-84, (2001) (PubMed).
Aliases for WFS1 抗体
wolframin ER transmembrane glycoprotein (Wfs1) 抗体wolframin ER transmembrane glycoprotein (WFS1) 抗体
wolfram syndrome 1 (wfs1) 抗体
wolframin (LOC552818) 抗体
wolfram syndrome 1 (CpipJ_CPIJ013087) 抗体
wolframin (WFS1) 抗体
Wolfram syndrome 1 (wolframin) L homeolog (wfs1.L) 抗体
AI481085 抗体
CG4917 抗体
Dmel\\CG4917 抗体
GB15257 抗体
WFRS 抗体
WFS 抗体
WFS1 抗体
wfs1 抗体
WFSL 抗体
wolframin 抗体
您还需要查找其他产品吗？
You are here:
