Congenital Heart Defect
Gene: TTC25EnsemblGeneIds (GRCh38): ENSG00000204815
EnsemblGeneIds (GRCh37): ENSG00000204815
OMIM: 617095, Gene2Phenotype
TTC25 is in 5 panels
1 review
Bryony Thompson (Royal Melbourne Hospital)
At least 3 probands reported with congenital heart defects and a supporting mouse model.
Sources: LiteratureCreated: 6 Jun 2023, 7:05 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
primary ciliary dyskinesia 35 MONDO:0014910
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- primary ciliary dyskinesia 35 MONDO:0014910
- Tags
- OMIM
- 617095
- Clinvar variants
- Variants in TTC25
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Added Tag
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Tag new gene name tag was added to gene: TTC25.
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: ttc25 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: ttc25 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: TTC25 was added gene: TTC25 was added to Congenital Heart Defect. Sources: Literature Mode of inheritance for gene: TTC25 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TTC25 were set to 34215651; 33746037; 27486780 Phenotypes for gene: TTC25 were set to primary ciliary dyskinesia 35 MONDO:0014910 Review for gene: TTC25 was set to GREEN