NRADDP
Description
The NRADDP (neurotrophin receptor associated death domain, pseudogene) is a pseudo gene located on chromosome 3.
NRADD1 is a gene that encodes a protein involved in the regulation of gene expression. It acts as a coactivator for several nuclear receptors, including the thyroid hormone receptor (TR), the retinoid X receptor (RXR), and the peroxisome proliferator-activated receptor (PPAR). NRAD1 is also thought to be involved in cellular differentiation and has been implicated in several developmental disorders, such as deafness, dysplasia, and intellectual disability.
NRADD1 (Nuclear Receptor Coactivator Associated with Deafness and Dysplasia) is a protein that in humans is encoded by the NRAD1 gene. It is thought to act as a coactivator for several nuclear receptors, such as the thyroid hormone receptor (TR), the retinoid X receptor (RXR), and the peroxisome proliferator-activated receptor (PPAR). NRAD1 is also believed to be involved in the regulation of gene expression and cellular differentiation. It has been implicated in several developmental disorders, including deafness, dysplasia, and intellectual disability.
NRADDP is also known as -.
