Coarse facial features including Coffin-Siris-like disorders
Gene: SOX11EnsemblGeneIds (GRCh38): ENSG00000176887
EnsemblGeneIds (GRCh37): ENSG00000176887
OMIM: 600898, Gene2Phenotype
SOX11 is in 8 panels
2 reviews
Alice Gardham (Genomics England)
Comment on list classification: Growing evidence that mutations are associated with Coffin Siris syndrome or Coffin Siris -like conditionCreated: 23 Nov 2016, 9:40 a.m.
alisdair mcneill (Sheffield childrens hospital)
de novo loss of function variants are associated with intellectual disability with coffin-siris featuresCreated: 29 Jun 2016, 6:56 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
coffin-siris; intellectual disability
Publications
- http://www.ncbi.nlm.nih.gov/pubmed/26543203
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Phenotypes
-
- coffin-siris syndrome
- OMIM
- 600898
- Clinvar variants
- Variants in SOX11
- Penetrance
- Complete
- Publications
-
- http://www.ncbi.nlm.nih.gov/pubmed/?term=mcneill+sox11
- Panels with this gene
History Filter Activity
Gene classified by Genomics England curator
Alice Gardham (Genomics England)This gene has been classified as Green List (High Evidence).
Gene classified by Genomics England curator
Alice Gardham (Genomics England)This gene has been classified as Green List (High Evidence).
Approved Gene
Ellen McDonagh (Genomics England Curator)This proposed gene was validated and added to this panel
Added New Source
alisdair mcneill (Sheffield childrens hospital)SOX11 was added to Coarse facial features including Coffin-Siris-like disorderspanel. Sources: Literature
Created
alisdair mcneill (Sheffield childrens hospital)SOX11 was created by [email protected]