Variants currently available for view at EAHAD Variant Coagulation Database

LOVD F8 homepage

General information
Gene name Coagulation factor VIII, procoagulant component
Gene symbol F8
Chromosome Location Xq28
Database location
Curator Daniel J Hampshire, Geoffrey Kemball-Cook, Keith Gomez and Pavithra Rallapalli
PubMed references View all (unique) PubMed references in the F8 database
Date of creation March 06, 2009
Last update October 26, 2012
Version F8 121026
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Reference sequence file coding DNA reference sequence for describing sequence variants
Genomic refseq ID NG_011403.1
Transcript refseq ID NM_000132.3
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 7
Total number of individuals with variant(s) 49
Total number of variants reported 49
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NOTE The work leading to the establishment of these LSDBs was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement nÂș 200754 - the GEN2PHEN project. This gene sequence variant databases (LSDBs) was initiated in connection with the study of Tarpey et al. (2009) A systematic, large-scale resequencing screen of the X-chromosome coding exons in mental retardation. Nat.Genet. 41: 535-543.

Graphical displays and utilities
Summary tables Summary of all sequence variants in the F8 database, sorted by type of variant (with graphical displays and statistics)
Reading-frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes
UCSC Genome Browser Show variants in the UCSC Genome Browser (compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Sequence variant tables
Unique sequence variants Listing of all unique sequence variants in the F8 database, without patient data
Complete sequence variant listing Listing of all sequence variants in the F8 database
Variants with no known pathogenicity Listing of all F8 variants reported to have no noticeable phenotypic effect (note: excluding variants of unknown effect)

Search the database
By type of variant View all sequence variants of a certain type
Simple search Query the database by selecting the most important variables (exon number, type of variant, disease phenotype)
Advanced search Query the database by selecting a combination of variables
Based on patient origin View all variants based on your patient origin search terms

Links to other resources
HGNC 3546
Entrez Gene 2157
OMIM - Gene 300841
OMIM - Disease hemophilia, type A (HEM-A)
UniProtKB (SwissProt/TrEMBL) P00451
GeneCards F8
GeneTests F8
External link Orphanet

Copyright & disclaimer
The contents of this LOVD database are the intellectual property of the respective curator(s). Any unauthorised use, copying, storage or distribution of this material without written permission from the curator(s) will lead to copyright infringement with possible ensuing litigation. Copyright © 2017. All Rights Reserved. For further details, refer to Directive 96/9/EC of the European Parliament and the Council of March 11 (1996) on the legal protection of databases.

We have used all reasonable efforts to ensure that the information displayed on these pages and contained in the databases is of high quality. We make no warranty, express or implied, as to its accuracy or that the information is fit for a particular purpose, and will not be held responsible for any consequences arising out of any inaccuracies or omissions. Individuals, organisations and companies which use this database do so on the understanding that no liability whatsoever either direct or indirect shall rest upon the curator(s) or any of their employees or agents for the effects of any product, process or method that may be produced or adopted by any part, notwithstanding that the formulation of such product, process or method may be based upon information here provided.