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
-
- Adult solid tumours cancer susceptibility
- Embryonal tumour of possible germline origin
- Primary lymphoedema
- Pneumothorax - familial
- Neurological segmental overgrowth
- Pigmentary skin disorders
- Fetal hydrops
- Hypertrophic cardiomyopathy
- Familial rhabdomyosarcoma
- Sarcoma of possible germline origin
- Monogenic short stature
- Hereditary neuropathy
- Congenital myopathy
- RASopathies
- IUGR and IGF abnormalities
- Early onset or syndromic epilepsy
- DDG2P
- Childhood solid tumours cancer susceptibility
- Intellectual disability
- Segmental overgrowth disorders - Deep sequencing
- Paediatric or syndromic cardiomyopathy
- Sarcoma cancer susceptibility
- Cytopenias and congenital anaemias
- Hereditary neuropathy or pain disorder
- Mosaic skin disorders - Deep sequencing
- Arthrogryposis
- Sarcoma susceptibility
- Fetal anomalies
- Childhood solid tumours
- Multiple monogenic benign skin 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