Childhood solid tumours
Gene: PIK3CA
PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha)
EnsemblGeneIds (GRCh38): ENSG00000121879
EnsemblGeneIds (GRCh37): ENSG00000121879
OMIM: 171834, Gene2Phenotype
PIK3CA is in 21 panels
EnsemblGeneIds (GRCh38): ENSG00000121879
EnsemblGeneIds (GRCh37): ENSG00000121879
OMIM: 171834, Gene2Phenotype
PIK3CA is in 21 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review
- Phenotypes
-
- 1 report of several families in PTEN-negative Cowden
- OMIM
- 171834
- Clinvar variants
- Variants in PIK3CA
- Penetrance
- Complete
- Publications
-
- PMID: 23246288
- Mode of Pathogenicity
- Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
- Panels with this gene
-
- Vascular skin disorders
- Multiple monogenic benign skin tumours
- Limb disorders
- Skeletal dysplasia
- Genodermatoses with malignancies
- Cerebral vascular malformations
- Beckwith-Wiedemann syndrome (BWS) and other congenital overgrowth disorders
- Malformations of cortical development
- Early onset or syndromic epilepsy
- Hydrocephalus
- Childhood solid tumours
- Familial Neural Tube Defects
- Segmental overgrowth disorders - Deep sequencing
- Intellectual disability
- Pigmentary skin disorders
- Mosaic skin disorders - deep sequencing
- Inherited non-medullary thyroid cancer
- Fetal anomalies
- DDG2P
- Neurological segmental overgrowth
- Hereditary haemorrhagic telangiectasia
History Filter Activity
28 Feb 2016, Gel status: 0
Added New Source
Ellen Thomas (Genomics England Curator)PIK3CA was added to Paediatric congenital malformation-dysmorphism-tumour syndromes panel. Sources: Expert Review
28 Feb 2016, Gel status: 0
Created
Ellen Thomas (Genomics England Curator)PIK3CA was created by EllenThomas