This Panel is marked as Deleted
Microcephaly Victorian Clinical Genetics Services
Gene: MRE11
MRE11 (MRE11 homolog, double strand break repair nuclease)
EnsemblGeneIds (GRCh38): ENSG00000020922
EnsemblGeneIds (GRCh37): ENSG00000020922
OMIM: 600814, Gene2Phenotype
MRE11 is in 17 panels
EnsemblGeneIds (GRCh38): ENSG00000020922
EnsemblGeneIds (GRCh37): ENSG00000020922
OMIM: 600814, Gene2Phenotype
MRE11 is in 17 panels
0 reviews
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 600814
- Clinvar variants
- Variants in MRE11
- Penetrance
- None
- Panels with this gene
-
- Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome
- Childhood onset dystonia, chorea or related movement disorder
- Severe microcephaly
- COVID-19 research
- Adult onset neurodegenerative disorder
- Intellectual disability
- Ataxia and cerebellar anomalies - narrow panel
- Fetal anomalies
- Hereditary ataxia with onset in adulthood
- Ductal plate malformation
- Hereditary neuropathy or pain disorder
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Hereditary ataxia
- DDG2P
- White matter disorders and cerebral calcification - narrow panel
- Hereditary neuropathy
- Hereditary haemorrhagic telangiectasia
History Filter Activity
21 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)MRE11 was added to Microcephaly Victorian Clinical Genetics Services panel. Sources: Expert Review Green,Victorian Clinical Genetics Services
21 Jun 2018, Gel status: 4
Created
Sarah Leigh (Genomics England Curator)MRE11 was created by Sarah Leigh