Osteogenesis imperfecta
Gene: EXT2EnsemblGeneIds (GRCh38): ENSG00000151348
EnsemblGeneIds (GRCh37): ENSG00000151348
OMIM: 608210, Gene2Phenotype
EXT2 is in 15 panels
3 reviews
Christine Burren (University Hospitals Bristol NHS Foundation Trust)
Rebecca Pollitt (Sheffield Diagnostic Genetics Service ; University of Sheffield)
Meena Balasubramanian (Sheffield Children's NHS Foundation Trust)
Remove from panelCreated: 27 Nov 2015, 3:04 p.m.
Details
- Sources
-
- Expert Review Removed
- Emory Genetics Laboratory
- Phenotypes
-
- Disproportionate Short Stature
- Tags
- OMIM
- 608210
- Clinvar variants
- Variants in EXT2
- Penetrance
- Complete
- Panels with this gene
-
- Congenital disorders of glycosylation
- Multiple exostoses
- Childhood onset dystonia, chorea or related movement disorder
- Sarcoma cancer susceptibility
- Undiagnosed metabolic disorders
- Skeletal dysplasia
- Early onset or syndromic epilepsy
- Adult solid tumours for rare disease
- Sarcoma susceptibility
- Osteogenesis imperfecta
- Likely inborn error of metabolism
- Intellectual disability
- Adult solid tumours cancer susceptibility
- Fetal anomalies
- DDG2P
History Filter Activity
Added Tag
Arina Puzriakova (Genomics England Curator)Tag curated_removed tag was added to gene: EXT2.
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been removed from the panel.
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been removed from the panel.
Added New Source
Ellen McDonagh (Genomics England Curator)EXT2 was added to Osteogenesis Imperfecta panel. Sources: Emory Genetics Laboratory