Mirror movements
Gene: DCCEnsemblGeneIds (GRCh38): ENSG00000187323
EnsemblGeneIds (GRCh37): ENSG00000187323
OMIM: 120470, Gene2Phenotype
DCC is in 6 panels
1 review
Bryony Thompson (Royal Melbourne Hospital)
Well-established and most common cause of congenital mirror movements. >20 cases reported.
Sources: Expert listCreated: 1 Sep 2021, 10:56 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Mirror movements 1 and/or agenesis of the corpus callosum MIM#157600
Publications
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Expert list
- Phenotypes
-
- Mirror movements 1 and/or agenesis of the corpus callosum MIM#157600
- OMIM
- 120470
- Clinvar variants
- Variants in DCC
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: dcc has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Bryony Thompson (Royal Melbourne Hospital)gene: DCC was added gene: DCC was added to Mirror movements. Sources: Expert list Mode of inheritance for gene: DCC was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: DCC were set to 20431009; 25763452; 28250454 Phenotypes for gene: DCC were set to Mirror movements 1 and/or agenesis of the corpus callosum MIM#157600 Review for gene: DCC was set to GREEN gene: DCC was marked as current diagnostic