Disease:Chromosomal aberrations involving RARA may be a cause of acute promyelocytic leukemia (APL) [MIM:612376]. Translocation t (11;17) (q32;q21) with ZBTB16/PLZF; translocation t (15;17) (q21;q21) with PML; translocation t (5;17) (q32;q11) with NPM. ,Domain:Composed of three domains: a modulating N-terminal domain , a DNA-binding domain and a C-terminal steroid-binding domain. ,Function:This is a receptor for retinoic acid. This metabolite has profound effects on vertebrate development. Retinoic acid is a morphogen and is a powerful teratogen. This receptor controls cell function by directly regulating gene expression. ,online information:Retinoic acid receptor entry ,PTM:Phosphorylated. Phosphorylation does not change during cell cycle. Phosphorylation on Ser-77 is crucial for transcriptional activity. ,similarity:Belongs to the nuclear hormone receptor family. ,similarity:Belongs to the nuclear hormone receptor family. NR1 subfamily. ,similarity:Contains 1 nuclear receptor DNA-binding domain. ,subunit:Interacts with CDK7 (By similarity) . Interacts with NCOA3 and NCOA6 coactivators , leading to a strong increase of transcription of target genes. Interacts with NOCA7 in a ligand-inducible manner. ,
展开内容