Familial Neural Tube Defects
Gene: GDF6EnsemblGeneIds (GRCh38): ENSG00000156466
EnsemblGeneIds (GRCh37): ENSG00000156466
OMIM: 601147, Gene2Phenotype
GDF6 is in 11 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Red
- Illumina TruGenome Clinical Sequencing Services
- Radboud University Medical Center, Nijmegen
- Phenotypes
-
- Klippel-Feil syndrome
- Klippel-Feil Syndrome
- OMIM
- 601147
- Clinvar variants
- Variants in GDF6
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
panel promoted to version 1
Ellen McDonagh (Genomics England Curator)25th Oct 2016: This panel was discussed internally, and as Neural tube defects (NTDs) are common multifactorial disorders caused by multiple genes and environmental factors, all genes on this panel should be considered red at this stage. Ready to promote to Version 1.
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Added New Source
Olivia Niblock (Genomics England Curator)GDF6 was added to Familial Neural Tube Defectspanel. Source: Illumina TruGenome Clinical Sequencing Services
Created
Olivia Niblock (Genomics England Curator)GDF6 was created by oniblock
Added New Source
Olivia Niblock (Genomics England Curator)GDF6 was added to Familial Neural Tube Defectspanel. Sources: Radboud University Medical Center, Nijmegen