Haematuria_Alport

Gene: FN1

Red List (low evidence)

FN1 (fibronectin 1)
EnsemblGeneIds (GRCh38): ENSG00000115414
EnsemblGeneIds (GRCh37): ENSG00000115414
OMIM: 135600, Gene2Phenotype
FN1 is in 5 panels

1 review

Chirag Patel (Genetic Health Queensland)

Red List (low evidence)

in proteinuria panel
Created: 3 Jan 2020, 5:07 a.m. | Last Modified: 3 Jan 2020, 5:07 a.m.
Panel Version: 0.17

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
135600
Clinvar variants
Variants in FN1
Penetrance
None
Panels with this gene

History Filter Activity

14 Jan 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: fn1 has been classified as Red List (Low Evidence).

3 Jan 2020, Gel status: 1

Entity classified by Genomics England curator

Chirag Patel (Genetic Health Queensland)

Gene: fn1 has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: FN1 was added gene: FN1 was added to Alport syndrome extended_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: FN1 was set to Unknown