KLHL21 Monoclonal Antibody, 100ul Plasma Defects in this gene are

Defects in this gene are also associated with early onset hypertension with severe exacerbation in pregnancy

|PTM:The vitamin K-dependent| enzymatic carboxylation of some glutamate residues allows the modified protein to bind calcium

Alternative splice variants have been described but their full length nature has not been determined

The expression of this receptor is induced by lymphocyte activation

KLHL21 Monoclonal Antibody, 100ul Plasma Defects in this gene areProbable substrate specific adapter of an E3 ubiquitin protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins.,pathway: Protein modification protein ubiquitination.,similarity: Contains 1 BACK (BTB Kelch associated) domain.,similarity: Contains 1 BTB (POZ) domain.,similarity: Contains 6 Kelch repeats.,subunit: Interacts with cul3.,