NCOR1


Summary: 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].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location

GO terms in NCOR1


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Term Type
Evidence Type
GO Term ID
GO Des.
CC IBA GO:0000118 histone deacetylase complex
CC IDA GO:0000118 histone deacetylase complex
CC IDA GO:0000790 nuclear chromatin
CC IBA GO:0005634 nucleus
CC IC GO:0005634 nucleus
CC IDA GO:0005634 nucleus
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Gene expression in normal tissue: NCOR1

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in NCOR1


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Database
Pathway ID
Pathway Des.
wikipathways WP138 Androgen receptor signaling pathway
wikipathways WP236 Adipogenesis
wikipathways WP34 Ovarian Infertility Genes
wikipathways WP3584 MECP2 and Associated Rett Syndrome
wikipathways WP3651 Pathways Affected in Adenoid Cystic Carcinoma
wikipathways WP61 Notch Signaling Pathway
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD264 Bryostatin 1 1
iGMDRD775 NCGC00346967-01 1
iGMDRD462 OSI-906 (Linsitinib) 1
iGMDRD441 TW 37 1
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in NCOR1

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

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