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  2. Paediatric motor neuronopathies
  3. MEG3
STRs in panel
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Paediatric motor neuronopathies

Gene: MEG3

Red List (low evidence)
MEG3 (maternally expressed 3 (non-protein coding))
EnsemblGeneIds (GRCh38): ENSG00000214548
EnsemblGeneIds (GRCh37): ENSG00000214548
OMIM: 605636, Gene2Phenotype
MEG3 is in 1 panel

2 reviews

Ellen McDonagh (Genomics England Curator)

Added tag to explain why there is no Ensembl gene ID for this entity.
Created: 6 Jan 2017, 3:42 p.m.
Created: 6 Jan 2017, 3:42 p.m.

Panel version: 0.38

Alice Gardham (Genomics England)

Comment on list classification: No known phenotype
Created: 2 Nov 2016, 2:46 p.m.
Created: 2 Nov 2016, 2:46 p.m.

Panel version: 0.23

Details

Sources
  • Expert Review Red
Tags
locus-type-rna-long-non-coding
OMIM
605636
Clinvar variants
Variants in MEG3
Penetrance
Complete
Panels with this gene

History Filter Activity

7 Mar 2017, Gel status: 1

panel promoted to version 1

Arianna Tucci (Genomics England Curator)

Gene panel promoted to v1 on 7 March 2017 following external review and internal curation

3 Nov 2016, Gel status: 1

Gene classified by Genomics England curator

Alice Gardham (Genomics England)

This gene has been classified as Red List (Low Evidence).

2 Nov 2016, Gel status: 1

Gene classified by Genomics England curator

Alice Gardham (Genomics England)

This gene has been classified as Red List (Low Evidence).

2 Nov 2016, Gel status: 1

clearsources

Alice Gardham (Genomics England)

MEG3All sources for gene: MEG3 were removed

30 Apr 2015, Gel status: 1

Added New Source

Antonio Rueda (GEL)

MEG3 was added to Paediatric motor neuronopathiespanel. Sources: Emory Genetics Laboratory