This Panel is marked as Deleted
Epileptic encephalopathy Victorian Clinical Genetics Services
Gene: HRAS
HRAS (HRas proto-oncogene, GTPase)
EnsemblGeneIds (GRCh38): ENSG00000174775
EnsemblGeneIds (GRCh37): ENSG00000174775
OMIM: 190020, Gene2Phenotype
HRAS is in 30 panels
EnsemblGeneIds (GRCh38): ENSG00000174775
EnsemblGeneIds (GRCh37): ENSG00000174775
OMIM: 190020, Gene2Phenotype
HRAS is in 30 panels
0 reviews
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 190020
- Clinvar variants
- Variants in HRAS
- Penetrance
- None
- Panels with this gene
-
- DDG2P
- Hereditary neuropathy or pain disorder
- Mosaic skin disorders - deep sequencing
- Fetal hydrops
- Familial rhabdomyosarcoma
- Paediatric or syndromic cardiomyopathy
- RASopathies
- IUGR and IGF abnormalities
- Hereditary neuropathy
- Childhood solid tumours cancer susceptibility
- Primary lymphoedema
- Sarcoma cancer susceptibility
- Cytopenias and congenital anaemias
- Intellectual disability
- Neurological segmental overgrowth
- Segmental overgrowth disorders - Deep sequencing
- Embryonal tumour of possible germline origin
- Multiple monogenic benign skin tumours
- Fetal anomalies
- Arthrogryposis
- Sarcoma susceptibility
- Hypertrophic cardiomyopathy
- Congenital myopathy
- Pigmentary skin disorders
- Early onset or syndromic epilepsy
- Adult solid tumours cancer susceptibility
- Monogenic short stature
- Childhood solid tumours
- Sarcoma of possible germline origin
- Pneumothorax - familial
History Filter Activity
12 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)HRAS was added to Epileptic encephalopathy Victorian Clinical Genetics Services panel. Sources: Expert Review Green,Victorian Clinical Genetics Services
12 Jun 2018, Gel status: 4
Created
Sarah Leigh (Genomics England Curator)HRAS was created by Sarah Leigh