CHDGene:ENSG00000032219
From CHDWiki
ARID4A
[edit] synopsis of the potential involvement in CHD
In a patient with a TGA, microtia, microphthalmia and polydactyly, a deletion on 14q21.3 was identified (Thienpont et al). Prioritisation of the genes in the deleted region resulted in a high ranking of ARID4A. Therefore the expression pattern of ARID4A was investigated in zebrafish. This showed only weak ubiquitous expression throughout development, suggesting that ARID4A does not play an important role in zebrafish cardiac development.External references for ARID4A
ensembl: ENSG00000032219
OMIM: 180201
Search miRBase for ARID4A
Expression patterns from 4DXPress: ARID4A
MGI: MGI:2444354
ZFIN:
Wikipedia: ARID4A
Search Wikiproteins: ARID4A
Search Genetic Association Database: ARID4A
Search GeneTests: ARID4A
CHeartED:
Known phenotypes for ARID4A
Non-syndromic
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Syndromic
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Protein interaction partners
Patients reports for ARID4A
- case 1301 Clinical data Phenotype
Translocations
| Region | References | OMIM | Comments |
|---|
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Mutations in ARID4A
| Mutation (DNA) | Mutation (peptide) | CHD | Reference | Other features | Inheritence | Additional info. |
Representation of protein ARID4A

Heart expression domain of ARID4A
No specified expression domain for ARID4A
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Associated CHDs found by automated text mining
AGeneApart Method
See complete results on Genopedia (including non CHD)
