The FGB gene homepage

General information
Gene symbol FGB
Gene name fibrinogen beta chain
Chromosome 4
Chromosomal band q28
Imprinted Unknown
Genomic reference NG_008833.1
Transcript reference NM_001184741.1, NM_005141.4
Associated with diseases afibrinogenemia, congenital, Dysfibrinogenemia, congenital
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 44
Unique public DNA variants reported 9
Individuals with public variants 29
Hidden variants -
Date created November 30, -0001
Date last updated September 28, 2016
Version FGB: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:3662
Entrez Gene 2244
PubMed articles FGB
OMIM - Gene 134830
OMIM - Diseases afibrinogenemia, congenital
Dysfibrinogenemia, congenital


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00028420 4 transcript variant 1 NM_005141.4 NP_005132.2 44
00028421 4 transcript variant 2 NM_001184741.1 NP_001171670.1 43