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Fetal anomalies

Gene: FGF20

Amber List (moderate evidence)

FGF20 (fibroblast growth factor 20)
EnsemblGeneIds (GRCh38): ENSG00000078579
EnsemblGeneIds (GRCh37): ENSG00000078579
OMIM: 605558, Gene2Phenotype
FGF20 is in 3 panels

1 review

Ain Roesley (Victorian Clinical Genetics Services)

I don't know

Multiple affected fetuses in a consanguineous family; functional data.
Created: 14 Feb 2022, 2:06 a.m. | Last Modified: 14 Feb 2022, 2:06 a.m.
Panel Version: 0.3396
Multiple affected fetuses in a consanguineous family; functional data.
Created: 14 Feb 2022, 2:06 a.m. | Last Modified: 14 Feb 2022, 2:06 a.m.
Panel Version: 0.3396

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Renal hypodysplasia/aplasia 2, MIM#615721

Publications

Variants in this GENE are reported as part of current diagnostic practice

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Genomics England PanelApp
Phenotypes
  • Renal hypodysplasia/aplasia 2, MIM#615721
OMIM
605558
Clinvar variants
Variants in FGF20
Penetrance
None
Publications
Panels with this gene

History Filter Activity

15 Feb 2022, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: fgf20 has been classified as Amber List (Moderate Evidence).

15 Feb 2022, Gel status: 2

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: FGF20 were changed from ?Renal hypodysplasia/aplasia 2, 615721 to Renal hypodysplasia/aplasia 2, MIM#615721

15 Feb 2022, Gel status: 2

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: fgf20 has been classified as Amber List (Moderate Evidence).

24 Oct 2021, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: FGF20 was added gene: FGF20 was added to Fetal anomalies. Sources: Expert Review Red,Genomics England PanelApp Mode of inheritance for gene: FGF20 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: FGF20 were set to 22698282; 23112089 Phenotypes for gene: FGF20 were set to ?Renal hypodysplasia/aplasia 2, 615721