The FGG gene homepage

General information
Gene symbol FGG
Gene name fibrinogen gamma chain
Chromosome 4
Chromosomal band q28
Imprinted Unknown
Genomic reference NG_008834.1
Transcript reference NM_000509.4, NM_021870.2
Associated with diseases afibrinogenemia, congenital, Dysfibrinogenemia, congenital
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 35
Unique public DNA variants reported 4
Individuals with public variants 34
Hidden variants 2
Date created November 30, -0001
Date last updated September 28, 2016
Version FGG:160928

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:3694
Entrez Gene 2266
PubMed articles FGG
OMIM - Gene 134850
OMIM - Diseases afibrinogenemia, congenital
Dysfibrinogenemia, congenital


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00048721 4 transcript variant gamma-B NM_021870.2 NP_068656.2 35
00029745 4 transcript variant gamma-A NM_000509.4 NP_000500.2 5