Genes in panel
Regions in panel
Prev Next

Mendeliome

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

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

I don't know

Multiple affected fetuses in a consanguineous family; functional data.
Sources: Expert Review
Created: 2 Sep 2021, 11:27 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Renal hypodysplasia/aplasia 2, MIM#615721

Publications

Details

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

History Filter Activity

2 Sep 2021, 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).

2 Sep 2021, 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).

2 Sep 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 Mendeliome. Sources: Expert Review Mode of inheritance for gene: FGF20 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: FGF20 were set to 22698282 Phenotypes for gene: FGF20 were set to Renal hypodysplasia/aplasia 2, MIM#615721 Review for gene: FGF20 was set to AMBER