Hydrops fetalis
Gene: RRAS2
RRAS2 (RAS related 2)
EnsemblGeneIds (GRCh38): ENSG00000133818
EnsemblGeneIds (GRCh37): ENSG00000133818
OMIM: 600098, Gene2Phenotype
RRAS2 is in 6 panels
EnsemblGeneIds (GRCh38): ENSG00000133818
EnsemblGeneIds (GRCh37): ENSG00000133818
OMIM: 600098, Gene2Phenotype
RRAS2 is in 6 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Established Rasopathy gene; identified in hydrops cohort PMID 33686258.
Sources: Expert ReviewCreated: 20 Oct 2022, 11:09 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Noonan syndrome 12 OMIM #618624
Publications
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Expert Review
- Phenotypes
-
- Noonan syndrome 12 OMIM #618624
- OMIM
- 600098
- Clinvar variants
- Variants in RRAS2
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
20 Oct 2022, Gel status: 3
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: rras2 has been classified as Green List (High Evidence).
20 Oct 2022, Gel status: 3
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: rras2 has been classified as Green List (High Evidence).
20 Oct 2022, Gel status: 1
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: RRAS2 was added gene: RRAS2 was added to Hydrops fetalis. Sources: Expert Review Mode of inheritance for gene: RRAS2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: RRAS2 were set to 33686258; 31130282 Phenotypes for gene: RRAS2 were set to Noonan syndrome 12 OMIM #618624 Review for gene: RRAS2 was set to GREEN