Ciliary Dyskinesia
Gene: ZMYND10EnsemblGeneIds (GRCh38): ENSG00000004838
EnsemblGeneIds (GRCh37): ENSG00000004838
OMIM: 607070, Gene2Phenotype
ZMYND10 is in 7 panels
2 reviews
Sebastian Lunke (Victorian Clinical Genetics Services)
Comment when marking as ready: More than 10 Families with hom and comp het variants and PCDCreated: 13 Jan 2020, 11:04 p.m. | Last Modified: 13 Jan 2020, 11:04 p.m.
Panel Version: 0.2
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Victorian Clinical Genetics Services
- Phenotypes
-
- Ciliary dyskinesia, primary, 22, MIM#615444
- OMIM
- 607070
- Clinvar variants
- Variants in ZMYND10
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: ZMYND10 were changed from to Ciliary dyskinesia, primary, 22, MIM#615444
Set publications
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Publications for gene: ZMYND10 were set to
Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Mode of inheritance for gene: ZMYND10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Entity classified by Genomics England curator
Sebastian Lunke (Victorian Clinical Genetics Services)Gene: zmynd10 has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: ZMYND10 was added gene: ZMYND10 was added to Ciliary dyskinesia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: ZMYND10 was set to Unknown