The FGG gene homepage

General information
Gene symbol FGG
Gene name fibrinogen gamma chain
Chromosome 4
Chromosomal band q32.1
Imprinted Unknown
Genomic reference NG_008834.1
Transcript reference NM_021870.2
Exon/intron information NM_021870.2 exon/intron table
Associated with diseases afibrinogenemia, congenital, Dysfibrinogenemia, congenital
Citation reference(s) PubMed: McVey et al., 2020
Refseq URL Genomic reference sequence
Curators (1) Daniel J Hampshire
Total number of public variants reported 18
Unique public DNA variants reported 11
Individuals with public variants 13
Hidden variants 0
Notes This version of the database is under construction. Please refer to the EAHAD Coagulation Factor Variant Databases for current listings.
Date created April 05, 2011
Date last updated September 17, 2021
Version FGG:210917

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_021870.2.
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
Homepage URL https://www.LOVD.nl/FGG
External URL EAHAD Coagulation Factor Variant Databases
HGNC 3694
Entrez Gene 2266
PubMed articles FGG
OMIM - Gene 134850
OMIM - Diseases afibrinogenemia, congenital
Dysfibrinogenemia, congenital
HGMD FGG
GeneCards FGG
GeneTests FGG
Orphanet FGG


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000107 4 fibrinogen gamma chain, transcript variant gamma-B NM_021870.2 NP_068656.2 18


Copyright & disclaimer
The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Mutation Databases are maintained and provided as a public service for the clinical, diagnostic and coagulation factor research communities. All individuals accessing and using the information contained in these mutation databases managed by EAHAD explicitly agree to abide by the database policy.

This version of the database is under construction. Please refer to the EAHAD Coagulation Factor Variant Databases for current listings.