The F10 gene homepage

General information
Gene symbol F10
Gene name coagulation factor X
Chromosome 13
Chromosomal band q34
Imprinted Unknown
Genomic reference NG_009258.1
Transcript reference NM_000504.3
Exon/intron information NM_000504.3 exon/intron table
Associated with diseases F10D
Citation reference(s) PubMed: McVey et al., 2020
Refseq URL Genomic reference sequence
Curators (1) Daniel J Hampshire
Total number of public variants reported 42
Unique public DNA variants reported 36
Individuals with public variants 0
Hidden variants -
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
Date last updated February 26, 2024
Version F10:240226

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_000504.3.
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/F10
External URL EAHAD Coagulation Factor Variant Databases
HGNC 3528
Entrez Gene 2159
PubMed articles F10
OMIM - Gene 613872
OMIM - Diseases F10D (deficiency, factor X (F10D))
HGMD F10
GeneCards F10
GeneTests F10
Orphanet F10


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00007346 13 coagulation factor X NM_000504.3 NP_000495.1 42


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.