Segmental overgrowth disorders - Deep sequencing
Gene: KRASEnsemblGeneIds (GRCh38): ENSG00000133703
EnsemblGeneIds (GRCh37): ENSG00000133703
OMIM: 190070, Gene2Phenotype
KRAS is in 30 panels
0 reviews
Details
- Sources
-
- Other
- Phenotypes
-
- Hemimegalencephaly
- Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic, 163200
- OMIM
- 190070
- Clinvar variants
- Variants in KRAS
- Penetrance
- Complete
- Panels with this gene
-
- Intellectual disability
- DDG2P
- Mosaic skin disorders - deep sequencing
- Pigmentary skin disorders
- Fetal hydrops
- Rare syndromic craniosynostosis or isolated multisuture synostosis
- Familial rhabdomyosarcoma
- RASopathies
- IUGR and IGF abnormalities
- Hereditary neuropathy
- Fetal anomalies
- Childhood solid tumours cancer susceptibility
- Primary lymphoedema
- Multiple monogenic benign skin tumours
- Sarcoma cancer susceptibility
- Early onset or syndromic epilepsy
- Cytopenias and congenital anaemias
- COVID-19 research
- Paediatric or syndromic cardiomyopathy
- Neurological segmental overgrowth
- Segmental overgrowth disorders - Deep sequencing
- Embryonal tumour of possible germline origin
- Hereditary neuropathy or pain disorder
- Sarcoma susceptibility
- Osteogenesis imperfecta
- Monogenic short stature
- Adult solid tumours cancer susceptibility
- Childhood solid tumours
- Sarcoma of possible germline origin
- Primary immunodeficiency or monogenic inflammatory bowel disease
History Filter Activity
panel promoted to version 1
Rebecca Foulger (Genomics England curator)28 November 2016: Reviews were assessed, and panel was revised according to expert review and additional curation.
Created
Rebecca Foulger (Genomics England curator)KRAS was created by rfoulger
Added New Source
Rebecca Foulger (Genomics England curator)KRAS was added to Regional overgrowth disorderspanel. Sources: Other