IUGR and IGF abnormalities
Gene: ORC6EnsemblGeneIds (GRCh38): ENSG00000091651
EnsemblGeneIds (GRCh37): ENSG00000091651
OMIM: 607213, Gene2Phenotype
ORC6 is in 8 panels
3 reviews
Peter Clayton (University of Manchester)
Philip Murray (University of Manchester)
emma baple (Genomics England Curator)
Comment on phenotypes: Meier GorlinCreated: 3 Apr 2016, 8:21 p.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Phenotypes
-
- Meier-Gorlin syndrome 3, OMIM:613803
- micrognathia, patellar aplasia/hypoplasia, microtia, mammary hypoplasia
- OMIM
- 607213
- Clinvar variants
- Variants in ORC6
- Penetrance
- Complete
- Publications
- Panels with this gene
History Filter Activity
Set Phenotypes
Arina Puzriakova (Genomics England Curator)Phenotypes for gene: ORC6 were changed from micrognathia, patellar aplasia/hypoplasia, microtia, mammary hypoplasia to Meier-Gorlin syndrome 3, OMIM:613803; micrognathia, patellar aplasia/hypoplasia, microtia, mammary hypoplasia
Gene classified by Genomics England curator
emma baple (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Set Phenotypes
emma baple (Genomics England Curator)Phenotypes for ORC6 were set to micrognathia, patellar aplasia/hypoplasia, microtia, mammary hypoplasia
Gene classified by Genomics England curator
emma baple (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Added New Source
Philip Murray (University of Manchester)ORC6 was added to IUGR and IGF abnormalitiespanel. Sources: Literature
Created
Philip Murray (University of Manchester)ORC6 was created by PhilMurray