Craniosynostosis
Gene: FGF10EnsemblGeneIds (GRCh38): ENSG00000070193
EnsemblGeneIds (GRCh37): ENSG00000070193
OMIM: 602115, Gene2Phenotype
FGF10 is in 8 panels
2 reviews
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Craniosynostosis
Publications
Tiong Tan (Victorian Clinical Genetics Services)
Comment on list classification: Two unrelated individuals in large craniosynostosis cohort with pathogenic variants in FGF10.Created: 9 Jun 2020, 12:27 a.m. | Last Modified: 9 Jun 2020, 12:27 a.m.
Panel Version: 0.38
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Amber
- Victorian Clinical Genetics Services
- Phenotypes
-
- Craniosynostosis
- OMIM
- 602115
- Clinvar variants
- Variants in FGF10
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: FGF10 were changed from to Craniosynostosis
Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Mode of inheritance for gene: FGF10 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Set publications
Tiong Tan (Victorian Clinical Genetics Services)Publications for gene: FGF10 were set to
Entity classified by Genomics England curator
Tiong Tan (Victorian Clinical Genetics Services)Gene: fgf10 has been classified as Amber List (Moderate Evidence).
Entity classified by Genomics England curator
Tiong Tan (Victorian Clinical Genetics Services)Gene: fgf10 has been classified as Amber List (Moderate Evidence).
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: FGF10 was added gene: FGF10 was added to Craniosynostosis_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: FGF10 was set to Unknown