Hydrops fetalis
Gene: CDK10EnsemblGeneIds (GRCh38): ENSG00000185324
EnsemblGeneIds (GRCh37): ENSG00000185324
OMIM: 603464, Gene2Phenotype
CDK10 is in 6 panels
1 review
Ain Roesley (Victorian Clinical Genetics Services)
1 out of 6 families reported hydrops
Sources: LiteratureCreated: 18 Apr 2022, 11:52 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Al Kaissi syndrome MIM#617694
Publications
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Amber
- Literature
- Phenotypes
-
- Al Kaissi syndrome MIM#617694
- OMIM
- 603464
- Clinvar variants
- Variants in CDK10
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Ain Roesley (Victorian Clinical Genetics Services)Gene: cdk10 has been classified as Amber List (Moderate Evidence).
Entity classified by Genomics England curator
Ain Roesley (Victorian Clinical Genetics Services)Gene: cdk10 has been classified as Amber List (Moderate Evidence).
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Ain Roesley (Victorian Clinical Genetics Services)gene: CDK10 was added gene: CDK10 was added to Hydrops fetalis. Sources: Literature Mode of inheritance for gene: CDK10 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CDK10 were set to 28886341; 34974531 Phenotypes for gene: CDK10 were set to Al Kaissi syndrome MIM#617694 Review for gene: CDK10 was set to AMBER gene: CDK10 was marked as current diagnostic