Osteogenesis imperfecta
Gene: EVC2EnsemblGeneIds (GRCh38): ENSG00000173040
EnsemblGeneIds (GRCh37): ENSG00000173040
OMIM: 607261, Gene2Phenotype
EVC2 is in 14 panels
2 reviews
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
- 607261
- Clinvar variants
- Variants in EVC2
- Penetrance
- Complete
- Panels with this gene
-
- Intellectual disability
- Gastrointestinal neuromuscular disorders
- DDG2P
- Skeletal dysplasia
- Thoracic dystrophies
- Primary ciliary disorders
- Limb disorders
- Rare multisystem ciliopathy disorders
- Neurological ciliopathies
- Fetal anomalies
- Skeletal ciliopathies
- Osteogenesis imperfecta
- Childhood onset dystonia, chorea or related movement disorder
- Ductal plate malformation
History Filter Activity
Added Tag
Arina Puzriakova (Genomics England Curator)Tag curated_removed tag was added to gene: EVC2.
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.
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)EVC2 was added to Osteogenesis Imperfecta panel. Sources: Emory Genetics Laboratory