Test MOI validation panel - do not edit
Gene: A2MEnsemblGeneIds (GRCh38): ENSG00000175899
EnsemblGeneIds (GRCh37): ENSG00000175899
OMIM: 103950, Gene2Phenotype
A2M is in 0 panels
1 review
Eleanor Williams (Genomics England Curator)
This gene has been added to the PanelApp test validation panel with a mode of inheritance that has incorrect casingCreated: 26 Jan 2020, 6:23 p.m. | Last Modified: 26 Jan 2020, 6:23 p.m.
Panel Version: 0.4
Details
- Mode of Inheritance
- MoNOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Green
- Phenotypes
-
- Allowed values MOI test - gene with non-standard MOI
- OMIM
- 103950
- Clinvar variants
- Variants in A2M
- Penetrance
- None
- Panels with this gene
-
History Filter Activity
Set Phenotypes
Eleanor Williams (Genomics England Curator)Phenotypes for gene: A2M were changed from Validation test gene, not for genome analysis to Allowed values MOI test - gene with non-standard MOI
Set Phenotypes
Eleanor Williams (Genomics England Curator)Phenotypes for gene: A2M were changed from to Validation test gene, not for genome analysis
Created, Added New Source, Set mode of inheritance
Eleanor Williams (Genomics England Curator)gene: A2M was added gene: A2M was added to PanelApp test validation panel. Sources: Expert Review Green Mode of inheritance for gene: A2M was set to MoNOALLELIC, autosomal or pseudoautosomal, imprinted status unknown