PLEK (pleckstrin) is a protein-coding gene. Diseases associated with PLEK include aarskog-scott syndrome, and centronuclear myopathy. GO annotations related to this gene include phosphatidylinositol-3,4-bisphosphate binding and protein homodimerization activity. An important paralog of this gene is PLEK2.
Function
phosphatidylinositol-3,4-bisphosphate binding; protein binding; protein homodimerization activity; protein kinase C binding;
Synonyms
PLEK; pleckstrin; P47; platelet 47 kDa protein;
Citations
Publication ()
Have you cited CDBP2326 in a publication? Let us know and earn a reward for your research.
Creative Diagnostics products are for RESEARCH USE ONLY, please make sure your review is research based.
Required fields are marked with *
Terms and conditions:
We will select high-quality review customers and offer a $30 coupon for your next purchase.
All product reviews must be submitted in the English language.
Creative Diagnostics will not share any personal information of applicants, and all information will be treated with strict confidentiality and will not be sold or disclosed to a third party.
COA
Publication 
Loading ......
