The F11 gene homepage

General information
Gene symbol F11
Gene name coagulation factor XI
Chromosome 4
Chromosomal band q35.2
Imprinted Unknown
Genomic reference NG_008051.1
Transcript reference NM_000128.3
Exon/intron information NM_000128.3 exon/intron table
Associated with diseases F11D
Citation reference(s) PubMed: McVey et al., 2020
Refseq URL Genomic reference sequence
Curators (1) Daniel J Hampshire
Total number of public variants reported 94
Unique public DNA variants reported 85
Individuals with public variants 65
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 29, 2010
Date last updated April 13, 2021
Version F11:210413

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_000128.3.
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 https://www.LOVD.nl/F11
External URL EAHAD Coagulation Factor Variant Databases
HGNC 3529
Entrez Gene 2160
PubMed articles F11
OMIM - Gene 264900
OMIM - Diseases F11D (deficiency, factor XI (F11D))
HGMD F11
GeneCards F11
GeneTests F11
Orphanet F11


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00007347 4 coagulation factor XI NM_000128.3 NP_000119.1 94


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.