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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- Adult solid tumours cancer susceptibility
- Paediatric or syndromic cardiomyopathy
- Early onset or syndromic epilepsy
- Embryonal tumour of possible germline origin
- Primary lymphoedema
- Neurological segmental overgrowth
- Intellectual disability
- Pigmentary skin disorders
- Fetal hydrops
- Familial rhabdomyosarcoma
- Hereditary neuropathy or pain disorder
- Sarcoma of possible germline origin
- Hereditary neuropathy
- RASopathies
- IUGR and IGF abnormalities
- DDG2P
- Monogenic short stature
- Childhood solid tumours cancer susceptibility
- Segmental overgrowth disorders - Deep sequencing
- Sarcoma cancer susceptibility
- Cytopenias and congenital anaemias
- COVID-19 research
- Osteogenesis imperfecta
- Mosaic skin disorders - Deep sequencing
- Sarcoma susceptibility
- Fetal anomalies
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Childhood solid tumours
- Multiple monogenic benign skin tumours
- Rare syndromic craniosynostosis or isolated multisuture synostosis
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