Adult solid tumours cancer susceptibility
Gene: EXT2EnsemblGeneIds (GRCh38): ENSG00000151348
EnsemblGeneIds (GRCh37): ENSG00000151348
OMIM: 608210, Gene2Phenotype
EXT2 is in 15 panels
1 review
Ellen McDonagh (Genomics England Curator)
This is a Green gene on the Adult solid tumours for rare disease (Version 1.21) gene panel, and was added to this panel for review.Created: 28 Mar 2019, 5:02 p.m.
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- NHS GMS
- Expert Review Amber
- Other
- Phenotypes
-
- Exostoses, multiple, type 2
- OMIM
- 608210
- Clinvar variants
- Variants in EXT2
- Penetrance
- None
- Publications
- Panels with this gene
-
- Undiagnosed metabolic disorders
- Multiple exostoses
- Congenital disorders of glycosylation
- Intellectual disability
- Early onset or syndromic epilepsy
- Childhood onset dystonia, chorea or related movement disorder
- DDG2P
- Sarcoma cancer susceptibility
- Skeletal dysplasia
- Likely inborn error of metabolism
- Adult solid tumours for rare disease
- Sarcoma susceptibility
- Osteogenesis imperfecta
- Adult solid tumours cancer susceptibility
- Fetal anomalies
History Filter Activity
Added New Source
Ivone Leong (Genomics England Curator)Source NHS GMS was added to EXT2.
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Ellen McDonagh (Genomics England Curator)gene: EXT2 was added gene: EXT2 was added to Adult solid tumours cancer susceptibility. Sources: Other,Expert Review Amber Mode of inheritance for gene: EXT2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: EXT2 were set to 27636706; 29529714; 23770606; 7726168 Phenotypes for gene: EXT2 were set to Exostoses, multiple, type 2