GeneID: 370
Names
Common Name: | Mi-2a | Type: | Gene |
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Chromosome: | 17 (NC_000017.11) | Locus: | NM_001005273.3 (CHD3) |
HUGO Symbol: | CHD3 | Full Name: | chromodomain helicase DNA binding protein 3 |
Exons: | 40 | Introns: | 39 |
Description:
This gene encodes a member of the CHD family of proteins which are characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD3 is a key component of NuRD, a protein complex that comprises both nucleosome remodeling and deacetylase activities. The NuRD complex has been associated with epigenetic mechanisms of transcriptional repression during development, and has been shown to play an important role in globin regulation.
Synonyms: ZFH , SNIBCPS , Mi2-ALPHA
Comments:
N/A
Number of entries/variants: 0
IthaScore
Publications / Origin
- Bauer DE, Kamran SC, Orkin SH, Reawakening fetal hemoglobin: prospects for new therapies for the β-globin disorders., Blood, 120(15), 2945-53, 2012
- Thein SL, Genetic association studies in β-hemoglobinopathies., Hematology Am Soc Hematol Educ Program, 2013(0), 354-61, 2013
- Hoffmeister H, Fuchs A, Erdel F, Pinz S, Gröbner-Ferreira R, Bruckmann A, Deutzmann R, Schwartz U, Maldonado R, Huber C, Dendorfer AS, Rippe K, Längst G, CHD3 and CHD4 form distinct NuRD complexes with different yet overlapping functionality., Nucleic Acids Res., 45(18), 10534-10554, 2017
A/A | Date | Curator(s) | Comments |
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1 | 2020-03-27 17:38:19 | The IthaGenes Curation Team | Created |