Respiratory ciliopathies including non-CF bronchiectasis
Gene: DNAH10EnsemblGeneIds (GRCh38): ENSG00000197653
EnsemblGeneIds (GRCh37): ENSG00000197653
OMIM: 605884, Gene2Phenotype
DNAH10 is in 1 panel
1 review
Achchuthan Shanmugasundram (Genomics England Curator)
The ClinGen Motile Ciliopathy expert panel has classified the association of autosomal recessive DNAH10 variants to primary ciliary dyskinesia (MONDO:0016575) as 'Limited'. More information can be found in https://search.clinicalgenome.org/CCID:008793.
Sources: ClinGenCreated: 14 Jul 2025, 2:54 p.m. | Last Modified: 14 Jul 2025, 3:07 p.m.
Panel Version: 4.28
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Spermatogenic failure 56, OMIM:619515; primary ciliary dyskinesia, MONDO:0016575
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- ClinGen
- Phenotypes
-
- Spermatogenic failure 56, OMIM:619515
- primary ciliary dyskinesia, MONDO:0016575
- OMIM
- 605884
- Clinvar variants
- Variants in DNAH10
- Penetrance
- None
- Panels with this gene
History Filter Activity
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Achchuthan Shanmugasundram (Genomics England Curator)gene: DNAH10 was added gene: DNAH10 was added to Respiratory ciliopathies including non-CF bronchiectasis. Sources: ClinGen Mode of inheritance for gene: DNAH10 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: DNAH10 were set to Spermatogenic failure 56, OMIM:619515; primary ciliary dyskinesia, MONDO:0016575 Review for gene: DNAH10 was set to RED