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Genomic imprinting v0.129 | MEG3 | Sarah Leigh Phenotypes for gene: MEG3 were changed from Kagami-Ogata syndrome, OMIM:608149; Temple syndrome, OMIM:616222 to Temple syndrome, OMIM:616222; Kagami-Ogata syndrome, OMIM:608149 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Genomic imprinting v0.128 | MEG3 | Sarah Leigh Publications for gene: MEG3 were set to 30794780; 18271756; http://igc.otago.ac.nz/home.html; 29641995 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Genomic imprinting v0.127 | MEG3 | Sarah Leigh Classified gene: MEG3 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Genomic imprinting v0.127 | MEG3 | Sarah Leigh Gene: meg3 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Genomic imprinting v0.126 | MEG3 | Sarah Leigh edited their review of gene: MEG3: Added comment: Not associated with a phenotype in OMIM, Gen2Phen or MONDO. The imprinted gene MEG3 has been associated with multiple cases of Temple syndrome (PMID: 33010492;33746039) and to Kagami-Ogata syndrome (PMID: 33067531).; Changed rating: GREEN; Changed publications to: 33010492, 33746039, 33067531 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Genomic imprinting v0.126 | MEG3 | Sarah Leigh Phenotypes for gene: MEG3 were changed from to Kagami-Ogata syndrome, OMIM:608149; Temple syndrome, OMIM:616222 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Genomic imprinting v0.48 | MEG3 | Sarah Leigh Publications for gene: MEG3 were set to 30794780; 18271756; http://igc.otago.ac.nz/home.html | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Genomic imprinting v0.26 | MEG3 | Sarah Leigh reviewed gene: MEG3: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Genomic imprinting v0.23 | MEG3 |
Sarah Leigh gene: MEG3 was added gene: MEG3 was added to Imprinted Genes. Sources: Literature Mode of inheritance for gene: MEG3 was set to MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed) Publications for gene: MEG3 were set to 30794780; 18271756; http://igc.otago.ac.nz/home.html |