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An interactive mutation database for human coagulation factor IX provides novel insights into the phenotypes and genetics of hemophilia B
Author(s) -
Rallapalli P. M.,
KemballCook G.,
Tuddenham E. G.,
Gomez K.,
Perkins S. J.
Publication year - 2013
Publication title -
journal of thrombosis and haemostasis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.947
H-Index - 178
eISSN - 1538-7836
pISSN - 1538-7933
DOI - 10.1111/jth.12276
Subject(s) - database , point mutation , phenotype , factor ix , genetics , mutation , gene , biology , computational biology , computer science
Summary Background Factor IX ( FIX ) is important in the coagulation cascade, being activated to FIX a on cleavage. Defects in the human F9 gene frequently lead to hemophilia B. Objective To assess 1113 unique F9 mutations corresponding to 3721 patient entries in a new and up‐to‐date interactive web database alongside the FIX a protein structure. Methods The mutations database was built using My SQL and structural analyses were based on a homology model for the human FIX a structure based on closely‐related crystal structures. Results Mutations have been found in 336 (73%) out of 461 residues in FIX . There were 812 unique point mutations, 182 deletions, 54 polymorphisms, 39 insertions and 26 others that together comprise a total of 1113 unique variants. The 64 unique mild severity mutations in the mature protein with known circulating protein phenotypes include 15 (23%) quantitative type I mutations and 41 (64%) predominantly qualitative type II mutations. Inhibitors were described in 59 reports (1.6%) corresponding to 25 unique mutations. Conclusion The interactive database provides insights into mechanisms of hemophilia B. Type II mutations are deduced to disrupt predominantly those structural regions involved with functional interactions. The interactive features of the database will assist in making judgments about patient management.