Identity
HGNC
LOCATION
17p13.1
LOCUSID
ALIAS
Mi-2a,Mi2-ALPHA,SNIBCPS,ZFH
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 1107
MIM: 602120
HGNC: 1918
Ensembl: ENSG00000170004
Variants:
dbSNP: 1107
ClinVar: 1107
TCGA: ENSG00000170004
COSMIC: CHD3
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38116750 | 2024 | A severe neurocognitive phenotype caused by biallelic CHD3 variants in two siblings. | 0 |
| 38116750 | 2024 | A severe neurocognitive phenotype caused by biallelic CHD3 variants in two siblings. | 0 |
| 37761804 | 2023 | Snijders Blok-Campeau Syndrome: Description of 20 Additional Individuals with Variants in CHD3 and Literature Review. | 0 |
| 37761804 | 2023 | Snijders Blok-Campeau Syndrome: Description of 20 Additional Individuals with Variants in CHD3 and Literature Review. | 0 |
| 35346573 | 2022 | Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome. | 8 |
| 35346573 | 2022 | Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome. | 8 |
| 33403747 | 2021 | Sequence and functional differences in the ATPase domains of CHD3 and SNF2H promise potential for selective regulability and drugability. | 0 |
| 33403747 | 2021 | Sequence and functional differences in the ATPase domains of CHD3 and SNF2H promise potential for selective regulability and drugability. | 0 |
| 32483341 | 2020 | A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome. | 15 |
| 32483341 | 2020 | A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome. | 15 |
| 30971721 | 2019 | A Multi-Trait Approach Identified Genetic Variants Including a Rare Mutation in RGS3 with Impact on Abnormalities of Cardiac Structure/Function. | 3 |
| 30971721 | 2019 | A Multi-Trait Approach Identified Genetic Variants Including a Rare Mutation in RGS3 with Impact on Abnormalities of Cardiac Structure/Function. | 3 |
| 30082317 | 2018 | The SUMO protease SENP1 and the chromatin remodeler CHD3 interact and jointly affect chromatin accessibility and gene expression. | 10 |
| 30082317 | 2018 | The SUMO protease SENP1 and the chromatin remodeler CHD3 interact and jointly affect chromatin accessibility and gene expression. | 10 |
| 28977666 | 2017 | CHD3 and CHD4 form distinct NuRD complexes with different yet overlapping functionality. | 47 |
Citation
Dessen P
CHD3 (chromodomain helicase DNA binding protein 3)
Atlas Genet Cytogenet Oncol Haematol. 2003-05-01
Online version: http://atlasgeneticsoncology.org/gene/40071/chd3-(chromodomain-helicase-dna-binding-protein-3)
