NR2C2 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human NR2C2 wild-type allele is located in the vicinity of 3p25 and is approximately 106 kb in length. This allele, which encodes nuclear receptor subfamily 2 group C member 2 protein, plays a role in hormone-mediated transcriptional regulation. Aberrant expression of the gene may be associated with corticotrophic malignancies and Cushing disease.

**Synonyms:** - Nuclear Receptor Subfamily 2, Group C, Member 2 wt Allele - TAK1 - TR2R1 - TR4 - hTAK1