Fetal hydrops
Gene: CDC42EnsemblGeneIds (GRCh38): ENSG00000070831
EnsemblGeneIds (GRCh37): ENSG00000070831
OMIM: 116952, Gene2Phenotype
CDC42 is in 9 panels
2 reviews
Sarah Leigh (Genomics England Curator)
There is only one paper that mentions fetal hydrops associated with CDC42 variants (PMID:33082562).Created: 9 Jul 2024, 12:40 p.m. | Last Modified: 9 Jul 2024, 12:40 p.m.
Panel Version: 1.72
Irina Adamena (Children's Clinical University Hospital)
Gene with strong evidence for fetal hydrops (PMID: 33082562)
Sources: LiteratureCreated: 11 Apr 2024, 3:43 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Nonimmune hydrops fetalis
Publications
- PMID: 33082562
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Amber
- Phenotypes
-
- Nonimmune hydrops fetalis
- OMIM
- 116952
- Clinvar variants
- Variants in CDC42
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Sarah Leigh (Genomics England Curator)Gene: cdc42 has been classified as Amber List (Moderate Evidence).
Set publications
Sarah Leigh (Genomics England Curator)Publications for gene: CDC42 were set to 3308256229335451; 26708094
Set publications
Sarah Leigh (Genomics England Curator)Publications for gene: CDC42 were set to 33082562
Set publications
Sarah Leigh (Genomics England Curator)Publications for gene: CDC42 were set to PMID: 33082562
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Irina Adamena (Children's Clinical University Hospital)gene: CDC42 was added gene: CDC42 was added to Fetal hydrops. Sources: Literature Mode of inheritance for gene: CDC42 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: CDC42 were set to PMID: 33082562 Phenotypes for gene: CDC42 were set to Nonimmune hydrops fetalis Review for gene: CDC42 was set to GREEN