Severe microcephaly
Gene: MED11EnsemblGeneIds (GRCh38): ENSG00000161920
EnsemblGeneIds (GRCh37): ENSG00000161920
OMIM: 612383, Gene2Phenotype
MED11 is in 5 panels
1 review
Sarah Leigh (Genomics England Curator)
Comment on list classification: There is enough evidence for this gene to be amber on the Severe microcephaly panel.Created: 4 Apr 2023, 2:58 p.m. | Last Modified: 4 Apr 2023, 2:58 p.m.
Panel Version: 4.3
Not associated with a phenotype in OMIM, but is associated with MED11-associated neurodevelopmental disorder in Gen2Phen. PMID: 36001086 reports a single MED11 variant (NM_001001683.4: c.325C>T, p.Arg109*), that segregates with the condition in five unrelated families, however, there is homozygosity between two of these families, idicating that they may be related. Global delay was observed in three individuals from three unrelated familes and seizures were evident in four individuals from four unrelated families. Severe microcephaly was apparent in the two unrelated familes where this parameter was recorded. Overall, the MED11-associated neurodevelopmental disorder appeared to result in profound effects and proved fatal at birth and 10 days in two of the cases reported.
Sources: LiteratureCreated: 4 Apr 2023, 2:45 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
MED11-associated neurodevelopmental disorder
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Amber
- Literature
- Phenotypes
-
- Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities, OMIM:620327
- OMIM
- 612383
- Clinvar variants
- Variants in MED11
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Set Phenotypes
Arina Puzriakova (Genomics England Curator)Phenotypes for gene: MED11 were changed from MED11-associated neurodevelopmental disorder to Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities, OMIM:620327
Removed Tag
Sarah Leigh (Genomics England Curator)Tag Q2_23_promote_green was removed from gene: MED11.
Entity classified by Genomics England curator
Sarah Leigh (Genomics England Curator)Gene: med11 has been classified as Amber List (Moderate Evidence).
Created, Added New Source, Added Tag, Set mode of inheritance, Set publications, Set Phenotypes
Sarah Leigh (Genomics England Curator)gene: MED11 was added gene: MED11 was added to Severe microcephaly. Sources: Literature Q2_23_promote_green tags were added to gene: MED11. Mode of inheritance for gene: MED11 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: MED11 were set to 36001086 Phenotypes for gene: MED11 were set to MED11-associated neurodevelopmental disorder Review for gene: MED11 was set to GREEN