FGA gene homepage

General information
Gene symbol FGA
Gene name fibrinogen alpha chain
Chromosome 4
Chromosomal band q31.3
Imprinted Unknown
Genomic reference NG_008832.1
Transcript reference NM_000508.3
Exon/intron information NM_000508.3 exon/intron table
Associated with diseases afibrinogenemia, congenital, amyloidosis, visceral (type VIII), Dysfibrinogenemia, congenital
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Daniel J Hampshire
Total number of public variants reported 10
Unique public DNA variants reported 8
Individuals with public variants 0
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 May 03, 2013

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_000508.3.
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 http://www.LOVD.nl/FGA
External URL EAHAD Coagulation Factor Variant Databases
Orphanet
HGNC 3661
Entrez Gene 2243
PubMed articles FGA
OMIM - Gene 134820
OMIM - Diseases afibrinogenemia, congenital
amyloidosis, visceral (type VIII)
Dysfibrinogenemia, congenital
HGMD FGA
GeneCards FGA
GeneTests FGA


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00007897 4 transcript variant alpha-E NM_000508.3 NP_000499.1 10


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.