Segmental overgrowth disorders - Deep sequencing
Gene: KRASEnsemblGeneIds (GRCh38): ENSG00000133703
EnsemblGeneIds (GRCh37): ENSG00000133703
OMIM: 190070, Gene2Phenotype
KRAS is in 30 panels
0 reviews
Details
- Sources
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- Other
- Phenotypes
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- Hemimegalencephaly
- Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic, 163200
- OMIM
- 190070
- Clinvar variants
- Variants in KRAS
- Penetrance
- Complete
- Panels with this gene
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- Multiple monogenic benign skin tumours
- Primary lymphoedema
- Adult solid tumours cancer susceptibility
- Osteogenesis imperfecta
- Mosaic skin disorders - deep sequencing
- Hereditary neuropathy
- Segmental overgrowth disorders - Deep sequencing
- Fetal hydrops
- Familial rhabdomyosarcoma
- Intellectual disability
- Sarcoma of possible germline origin
- RASopathies
- IUGR and IGF abnormalities
- Pigmentary skin disorders
- Early onset or syndromic epilepsy
- Childhood solid tumours cancer susceptibility
- Embryonal tumour of possible germline origin
- Monogenic short stature
- Hereditary neuropathy or pain disorder
- Sarcoma cancer susceptibility
- Cytopenias and congenital anaemias
- COVID-19 research
- Neurological segmental overgrowth
- Sarcoma susceptibility
- Rare syndromic craniosynostosis or isolated multisuture synostosis
- DDG2P
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Childhood solid tumours
- Fetal anomalies
- Paediatric or syndromic cardiomyopathy
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