IUGR and IGF abnormalities
Gene: HRASEnsemblGeneIds (GRCh38): ENSG00000174775
EnsemblGeneIds (GRCh37): ENSG00000174775
OMIM: 190020, Gene2Phenotype
HRAS is in 30 panels
2 reviews
Philip Murray (University of Manchester)
Peter Clayton (University of Manchester)
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Phenotypes
-
- Costello syndrome
- OMIM
- 190020
- Clinvar variants
- Variants in HRAS
- Penetrance
- Complete
- Publications
- Panels with this gene
-
- Paediatric or syndromic cardiomyopathy
- Multiple monogenic benign skin tumours
- Primary lymphoedema
- Hypertrophic cardiomyopathy
- Adult solid tumours cancer susceptibility
- Mosaic skin disorders - deep sequencing
- DDG2P
- Hereditary neuropathy
- Arthrogryposis
- Segmental overgrowth disorders - Deep sequencing
- Fetal hydrops
- Familial rhabdomyosarcoma
- Sarcoma of possible germline origin
- Congenital myopathy
- RASopathies
- IUGR and IGF abnormalities
- Pigmentary skin disorders
- Childhood solid tumours cancer susceptibility
- Embryonal tumour of possible germline origin
- Intellectual disability
- Monogenic short stature
- Hereditary neuropathy or pain disorder
- Early onset or syndromic epilepsy
- Sarcoma cancer susceptibility
- Cytopenias and congenital anaemias
- Pneumothorax - familial
- Neurological segmental overgrowth
- Fetal anomalies
- Sarcoma susceptibility
- Childhood solid tumours
History Filter Activity
Gene classified by Genomics England curator
emma baple (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Gene classified by Genomics England curator
emma baple (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Added New Source
Peter Clayton (University of Manchester)HRAS was added to IUGR and IGF abnormalitiespanel. Sources: Literature
Created
Peter Clayton (University of Manchester)HRAS was created by peter.clayton