NCOR1

This gene encodes a protein that mediates ligand-independent transcription repression of thyroid-hormone and retinoic-acid receptors by promoting chromatin condensation and preventing access of the transcription machinery. It is part of a complex which also includes histone deacetylases and transcriptional regulators similar to the yeast protein Sin3p. This gene is located between the Charcot-Marie-Tooth and Smith-Magenis syndrome critical regions on chromosome 17. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 17 and 20. [provided by RefSeq, Jun 2010]

Description

nuclear receptor corepressor 1

Protein family

Cancer-related genes, Mapped to UniProt SWISS-PROT, Plasma proteins, Predicted intracellular proteins, Protein evidence (Ezkurdia et al 2014), Protein evidence (Kim et al 2014), Transcription factors

Chromosome

17 (16029157 - 16218185)

Ensembl ID

ENSG00000141027  (ver. 84.38)

Orthologs

Mouse Ncor1: ENSMUSG00000018501

UniProt

O75376

neXtProt

NX_O75376

Human splice variants
Mouse splice variants