This Panel is marked as Deleted
Renal cystic disease_SuperPanel_KidGen_VCGS
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
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Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Green
- KidGen_Cystic v38.1.0
- OMIM
- 191092
- Clinvar variants
- Variants in TSC2
- Penetrance
- None
- Panels with this gene
-
- Familial pulmonary fibrosis
- DDG2P
- Fetal anomalies
- Mosaic skin disorders - deep sequencing
- Early onset or syndromic epilepsy
- Classical tuberous sclerosis
- Adult solid tumours for rare disease
- Malformations of cortical development
- Intellectual disability
- Multiple monogenic benign skin tumours
- Unexplained kidney failure in young people
- Adult solid tumours cancer susceptibility
- Rare multisystem ciliopathy disorders
- Pigmentary skin disorders
- Cystic kidney disease
- Childhood solid tumours
- Skeletal dysplasia
- Pneumothorax - familial
- Tuberous sclerosis
- Ehlers Danlos syndrome with a likely monogenic cause
- Thoracic dystrophies
- Primary ciliary disorders
- Structural eye disease
- Childhood solid tumours cancer susceptibility
- Primary lymphoedema
History Filter Activity
23 Dec 2019, Gel status: 3
Created, Added New Source, Set mode of inheritance
Ivone Leong (Genomics England Curator)gene: TSC2 was added gene: TSC2 was added to Renal cystic disease_SuperPanel_KidGen_VCGS. Sources: KidGen_Cystic v38.1.0,Expert Review Green Mode of inheritance for gene: TSC2 was set to Unknown