This Panel is marked as Retired
Multiple Tumours
Gene: TSC2
TSC2 (TSC complex subunit 2)
EnsemblGeneIds (GRCh38): ENSG00000103197
EnsemblGeneIds (GRCh37): ENSG00000103197
OMIM: 191092, Gene2Phenotype
TSC2 is in 25 panels
EnsemblGeneIds (GRCh38): ENSG00000103197
EnsemblGeneIds (GRCh37): ENSG00000103197
OMIM: 191092, Gene2Phenotype
TSC2 is in 25 panels
1 review
Ellen McDonagh (Genomics England Curator)
Information from TruSight panel: Pathogenic Mutations are Inactivating.Created: 5 Feb 2016, 11:47 a.m.
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- TruSight Cancer Panel (Illumina)
- Phenotypes
-
- Tuberous sclerosis 2Renal cell cancer, angiomyolipoma
- Subependymal giant cell astrocytoma
- Rhabdomyoma (cardiac)
- Hamartoma (retinal, gastrointestinal tract)
- Paediatric congenital malformation-dysmorphism-tumour syndromes
- OMIM
- 191092
- Clinvar variants
- Variants in TSC2
- Penetrance
- Complete
- Panels with this gene
-
- Classical tuberous sclerosis
- Adult solid tumours for rare disease
- Skeletal dysplasia
- Intellectual disability
- Unexplained kidney failure in young people
- DDG2P
- Rare multisystem ciliopathy disorders
- Cystic kidney disease
- Childhood solid tumours
- Pigmentary skin disorders
- Fetal anomalies
- Tuberous sclerosis
- Early onset or syndromic epilepsy
- Thoracic dystrophies
- Primary ciliary disorders
- Childhood solid tumours cancer susceptibility
- Structural eye disease
- Multiple monogenic benign skin tumours
- Primary lymphoedema
- Adult solid tumours cancer susceptibility
- Malformations of cortical development
- Familial pulmonary fibrosis
- Mosaic skin disorders - deep sequencing
- Ehlers Danlos syndrome with a likely monogenic cause
- Pneumothorax - familial
History Filter Activity
9 Mar 2016, Gel status: 4
Set Mode of Inheritance, Added New Source
Ellen McDonagh (Genomics England Curator)TSC2 was added to Multiple Tumourspanel. Source: Expert Review Green Model of inheritance for gene TSC2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
5 Feb 2016, Gel status: 0
Added New Source
Ellen McDonagh (Genomics England Curator)TSC2 was added to Multiple Tumourspanel. Sources: TruSight Cancer Panel (Illumina)
5 Feb 2016, Gel status: 0
Created
Ellen McDonagh (Genomics England Curator)TSC2 was created by ellenmcdonagh