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  2. Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic
  3. FGF20
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Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic

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 list
Created: 28 Nov 2019, 5:40 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Renal hypodysplasia/aplasia 2, MIM#615721

Publications

Created: 28 Nov 2019, 5:40 a.m.

Panel version: 0.15

Details

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

History Filter Activity

28 Nov 2019, 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).

28 Nov 2019, 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).

28 Nov 2019, 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 Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic_VCGS. Sources: Expert list 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