Periodic fever syndromes
Gene: FGA
Comment on list classification: Mutations are 5' end of exon5Created: 2 Feb 2017, 1:29 p.m.
Many reported cases of FGA amyloidosis. Suggested gene in entry criteria for this gene panelCreated: 30 Jan 2017, 4:46 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Amyloidosis, familial visceral 105200
Publications
Phenotypes for gene: FGA were changed from Amyloidosis, familial visceral 105200 to Amyloidosis, familial visceral, OMIM:105200
22nd February 2017: Promoted to V1. Panel was reviewed by Tracy Briggs and Alice Gardham. Panel was revised according to expert review and additional curation.
Mode of inheritance for FGA was changed to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
This gene has been classified as Green List (High Evidence).
This gene has been classified as Green List (High Evidence).
Phenotypes for FGA were set to Amyloidosis, familial visceral 105200
Publications for FGA were set to 8097946
This gene has been classified as Green List (High Evidence).
FGA was added to Periodic fever syndromes and amyloidosis panel. Sources: Eligibility statement prior genetic testing
Model of inheritance for gene FGA was changed to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
FGA was added to Periodic fever syndromes and amyloidosis panel. Sources: Radboud University Medical Center, Nijmegen,Illumina TruGenome Clinical Sequencing Services,Eligibility Statements for GeL
Model of inheritance for gene FGA was changed to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
FGA was added to Periodic fever syndromes and amyloidosis panel. Sources: Radboud University Medical Center, Nijmegen,Illumina TruGenome Clinical Sequencing Services,Eligibility Statements for GeL
FGA was added to Periodic fever syndromes and amyloidosis panel. Sources: Radboud University Medical Center, Nijmegen,Illumina TruGenome Clinical Sequencing Services,Eligibility Statements for GeL