Microcephaly
Gene: TRAIPEnsemblGeneIds (GRCh38): ENSG00000183763
EnsemblGeneIds (GRCh37): ENSG00000183763
OMIM: 605958, Gene2Phenotype
TRAIP is in 6 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Three families reported, though two distantly related (founder); functional data.Created: 2 Apr 2021, 4:35 a.m. | Last Modified: 2 Apr 2021, 4:35 a.m.
Panel Version: 0.623
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Seckel syndrome 9, MIM# 616777
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Victorian Clinical Genetics Services
- Phenotypes
-
- Seckel syndrome 9, MIM# 616777
- OMIM
- 605958
- Clinvar variants
- Variants in TRAIP
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: traip has been classified as Green List (High Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: TRAIP were changed from to Seckel syndrome 9, MIM# 616777
Set publications
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Publications for gene: TRAIP were set to
Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Mode of inheritance for gene: TRAIP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: TRAIP was added gene: TRAIP was added to Microcephaly_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: TRAIP was set to Unknown