Cataract
Gene: CD3GEnsemblGeneIds (GRCh38): ENSG00000160654
EnsemblGeneIds (GRCh37): ENSG00000160654
OMIM: 186740, Gene2Phenotype
CD3G is in 5 panels
1 review
Lauren Akesson (Royal Melbourne Hospital)
Cataracts are not a typical feature of this condition (OMIM, PubMed: reviewed in PMID 31921117)Created: 20 Mar 2020, 4:56 a.m. | Last Modified: 20 Mar 2020, 4:56 a.m.
Panel Version: 0.22
Phenotypes
Immunodeficiency 17, CD3 gamma deficient
Publications
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Red
- Victorian Clinical Genetics Services
- Phenotypes
-
- Immunodeficiency 17, CD3 gamma deficient
- OMIM
- 186740
- Clinvar variants
- Variants in CD3G
- 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: cd3g has been classified as Red List (Low Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: CD3G were changed from to Immunodeficiency 17, CD3 gamma deficient
Set publications
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Publications for gene: CD3G were set to
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: cd3g has been classified as Red List (Low Evidence).
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: CD3G was added gene: CD3G was added to Cataract_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: CD3G was set to Unknown