Tumour predisposition - adult onset
Gene: EXT2EnsemblGeneIds (GRCh38): ENSG00000151348
EnsemblGeneIds (GRCh37): ENSG00000151348
OMIM: 608210, Gene2Phenotype
EXT2 is in 15 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Adult solid tumours for rare disease (Version 1.21)
- Phenotypes
-
- Exostoses, multiple, type 2 133701
- OMIM
- 608210
- Clinvar variants
- Variants in EXT2
- Penetrance
- None
- Publications
- Panels with this gene
-
- Intellectual disability
- Multiple exostoses
- Skeletal dysplasia
- Sarcoma cancer susceptibility
- DDG2P
- Undiagnosed metabolic disorders
- Fetal anomalies
- Adult solid tumours for rare disease
- Early onset or syndromic epilepsy
- Sarcoma susceptibility
- Osteogenesis imperfecta
- Adult solid tumours cancer susceptibility
- Congenital disorders of glycosylation
- Childhood onset dystonia, chorea or related movement disorder
- Likely inborn error of metabolism
History Filter Activity
Panel promoted to version 1.0
Rebecca Foulger (Genomics England curator)Panel checked against two component panels (Adult solid tumours for rare disease v1.21 and Familial Tumours Syndromes of the central & peripheral Nervous system v1.8) and promoted to Version 1.0.
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Rebecca Foulger (Genomics England curator)gene: EXT2 was added gene: EXT2 was added to Tumour predisposition - adult onset. Sources: Adult solid tumours for rare disease (Version 1.21),Expert Review Green Mode of inheritance for gene: EXT2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: EXT2 were set to 7726168; 23770606 27636706; 29529714 Phenotypes for gene: EXT2 were set to Exostoses, multiple, type 2 133701