Clefting
Gene: TGDSEnsemblGeneIds (GRCh38): ENSG00000088451
EnsemblGeneIds (GRCh37): ENSG00000088451
OMIM: 616146, Gene2Phenotype
TGDS is in 6 panels
1 review
Helen Brittain (Genomics England Curator)
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
CATEL-MANZKE SYNDROME; CATMANS
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- Phenotypes
-
- CATEL-MANZKE SYNDROME
- CATMANS
- Cleft palate
- OMIM
- 616146
- Clinvar variants
- Variants in TGDS
- Penetrance
- Complete
- Publications
- Panels with this gene
History Filter Activity
Added New Source, Set penetrance
Ellen McDonagh (Genomics England Curator)Victorian Clinical Genetics Services was added to TGDS. Panel: Clefting Phenotypes for gene TGDS were set to CATEL-MANZKE SYNDROME, CATMANS, Cleft palate
panel promoted to version 1
Louise Daugherty (Genomics England Curator)Panel reviews were assessed, and panel was revised according to reviews and further curation 31st May 2017
Added New Source
Ellen McDonagh (Genomics England Curator)TGDS was added to Cleftingpanel. Sources: Expert Review Green
Created
Ellen McDonagh (Genomics England Curator)TGDS was created by ellenmcdonagh