Rasopathy
Gene: RRAS2EnsemblGeneIds (GRCh38): ENSG00000133818
EnsemblGeneIds (GRCh37): ENSG00000133818
OMIM: 600098, Gene2Phenotype
RRAS2 is in 6 panels
1 review
Alison Yeung (Victorian Clinical Genetics Services)
Six unrelated families reported
Sources: LiteratureCreated: 20 Jan 2020, 4:59 a.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Noonan syndrome 12 OMIM #618624
Publications
- PMID: 31130282
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- Noonan syndrome 12 OMIM #618624
- OMIM
- 600098
- Clinvar variants
- Variants in RRAS2
- Penetrance
- None
- Publications
-
- PMID: 31130282
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Alison Yeung (Victorian Clinical Genetics Services)Gene: rras2 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Alison Yeung (Victorian Clinical Genetics Services)Gene: rras2 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Alison Yeung (Victorian Clinical Genetics Services)Gene: rras2 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Alison Yeung (Victorian Clinical Genetics Services)Gene: rras2 has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Alison Yeung (Victorian Clinical Genetics Services)gene: RRAS2 was added gene: RRAS2 was added to Rasopathy. Sources: Literature Mode of inheritance for gene: RRAS2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: RRAS2 were set to PMID: 31130282 Phenotypes for gene: RRAS2 were set to Noonan syndrome 12 OMIM #618624 Review for gene: RRAS2 was set to GREEN