Congenital Heart Defect
Gene: ZMYND10EnsemblGeneIds (GRCh38): ENSG00000004838
EnsemblGeneIds (GRCh37): ENSG00000004838
OMIM: 607070, Gene2Phenotype
ZMYND10 is in 7 panels
1 review
Bryony Thompson (Royal Melbourne Hospital)
CHD is a commonly reported feature of the condition.
Sources: OtherCreated: 7 Jun 2023, 3:08 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Primary ciliary dyskinesia 22 MONDO:0014192
Publications
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Other
- Phenotypes
-
- Primary ciliary dyskinesia 22 MONDO:0014192
- OMIM
- 607070
- Clinvar variants
- Variants in ZMYND10
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: zmynd10 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: zmynd10 has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Bryony Thompson (Royal Melbourne Hospital)gene: ZMYND10 was added gene: ZMYND10 was added to Congenital Heart Defect. Sources: Other Mode of inheritance for gene: ZMYND10 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: ZMYND10 were set to 23891471; 23891469; 29402277 Phenotypes for gene: ZMYND10 were set to Primary ciliary dyskinesia 22 MONDO:0014192 Review for gene: ZMYND10 was set to GREEN gene: ZMYND10 was marked as current diagnostic