MEG3

maternally expressed 3 (non-protein coding)
OMIM: 605636, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green MEG3 in Genomic imprinting


Version 0.149

review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Temple syndrome, OMIM:616222
  • Kagami-Ogata syndrome, OMIM:608149
Red MEG3 in Paediatric motor neuronopathies

Level 3: Motor and Sensory Disorders of the PNS
Level 2: Neurology and neurodevelopmental disorders
Version 3.7
Latest signed off version: v3.6 (1 May 2024)

Component of the following Super Panels:

  • Hypotonic infant
  • Other rare neuromuscular disorders
  • review Not set
    Sources
    • Expert Review Red
    Tags
    • locus-type-rna-long-non-coding