MEG3

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

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green MEG3 in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Kagami-Ogata syndrome, MIM# 608149
Tags
  • SV/CNV
  • non-coding gene

Green MEG3 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.83

review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Kagami-Ogata syndrome, MIM# 608149

Green MEG3 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 0.305

review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Kagami-Ogata syndrome, MIM# 608149
Tags
  • SV/CNV
  • non-coding gene

Green MEG3 in Imprinting disorders


Version 1.5

review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Kagami-Ogata syndrome, MIM# 608149
Tags
  • SV/CNV
  • non-coding gene