ROR Alpha Polyclonal Antibody, 100ul Modification Enzymes Mutations in this gene cause

Mutations in this gene cause congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency

and parathyroid carcinoma

interacting with nuclear transcription factor Y to activate UPR target genes

Three alternatively spliced transcript variants encoding different isoforms have been found for this gene

CR1 (complement C3b/C4b receptor 1 (Knops blood group)) is a member of the receptors of complement activation (RCA) family and is located in the 'cluster RCA' region of chromosome 1

ROR Alpha Polyclonal Antibody, 100ul Modification Enzymes Mutations in this gene causeNuclear receptor ROR alpha encoded by RORA is a member of the NR1 subfamily of nuclear hormone receptors. It can bind as a monomer or as a homodimer to hormone response elements upstream of several genes to enhance the expression of those genes. The encoded protein has been shown to interact with NM23 2, a nucleoside diphosphate kinase involved in organogenesis and differentiation, as well as with NM23 1, the product of a tumor metastasis suppressor