factorix.org

Factor IX Variant Database

Haemophilia B is caused by Variants mutations in the F9. Gene which codes for coagulation factor IX. There are currently 1095. Unique variants in the F9. Gene compiled within this database corresponding to 3713. If you find this website useful, please reference our publication. What can you do in this database? You can search for all the mutations reported in the F9. Simple Amino Acid Search. Exon and Intron based search. CodonAmino-acid numbering HGVS and Legacy. We are grateful for Dr Peter Green.
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FACTORIX.ORG HISTORY

The web site factorix.org was began on on April 04, 2012. It is now six hundred and thirty-nine weeks, two days, twelve hours, and fifty minutes old.
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LINKS TO FACTORIX.ORG

EAHAD VARIANT DATABASES

The intention of this project is to gather together single gene variant databases involved in clinical bleeding disorders, principally haemophilias A and B and von Willebrand disease, as well as other rarer coagulation factor variants. You may use this portal either to search for reports of known variants, or to submit your own reports for inclusion.

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CONTACTS

UCL

Stephen Perkins

Department of Structural and Molecular Biology

London, London, WC1E 6BT

GB

44.2076797048
s.perkins@ucl.ac.uk

FACTORIX.ORG SERVER

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SITE TITLE

Factor IX Variant Database

DESCRIPTION

Haemophilia B is caused by Variants mutations in the F9. Gene which codes for coagulation factor IX. There are currently 1095. Unique variants in the F9. Gene compiled within this database corresponding to 3713. If you find this website useful, please reference our publication. What can you do in this database? You can search for all the mutations reported in the F9. Simple Amino Acid Search. Exon and Intron based search. CodonAmino-acid numbering HGVS and Legacy. We are grateful for Dr Peter Green.

PARSED CONTENT

The web site factorix.org states the following, "Haemophilia B is caused by Variants mutations in the F9." I noticed that the webpage also said " Gene which codes for coagulation factor IX." They also said " Unique variants in the F9. Gene compiled within this database corresponding to 3713. If you find this website useful, please reference our publication. What can you do in this database? You can search for all the mutations reported in the F9. Exon and Intron based search. CodonAmino-acid numbering HGVS and Legacy. We are grateful for Dr Peter Green."

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