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