TY - JOUR
T1 - The infevers autoinflammatory mutation online registry
T2 - Update with new genes and functions
AU - Milhavet, Florian
AU - Cuisset, Laurence
AU - Hoffman, Hal M.
AU - Slim, Rima
AU - El-Shanti, Hatem
AU - Aksentijevich, Ivona
AU - Lesage, Suzanne
AU - Waterham, Hans
AU - Wise, Carol
AU - De Menthiere, Cyril Sarrauste
AU - Touitou, Isabelle
PY - 2008/6
Y1 - 2008/6
N2 - Infevers (Internet Fevers; http://fmf.igh.cnrs.fr/ISSAID/infevers), a website dedicated to mutations responsible for hereditary autoinflammatory diseases, was created in 2002 and has continued to evolve. This new version includes eight genes; six were already present: MEFV, MVK, TNFRSF1A, NLRP3, NOD2, PSTPIP1, and two are new, LPIN2 and NLRP7. Currently, Infevers contains over 540 sequence variants. Several new database functions were recently instituted. The website now accepts confidential data and complex alleles. For each gene, a newly created menu offers: 1) a tabular list of the variants that can be sorted by several parameters; 2) a gene graph providing a schematic representation of the variants along the gene; 3) statistical analysis of the data according to the phenotype, alteration type, and location of the mutation in the gene; 4) the cDNA and gDNA sequences of each gene, showing the nucleotide changes along the sequence, with a color-based code highlighting the gene domains, the first ATG, and the termination codon; and 5) a "download" menu making all tables and figures available for the users, which, except for the gene graphs, are all automatically generated and updated upon submission of the variants. Finally, the entire database was curated to comply with the HUGO Gene Nomenclature Committee (HGNC) and HGVS nomenclature guidelines, and wherever necessary, an informative note was provided. Infevers has already proven useful for the scientific community with a mean number of visits per month of 200 in 2002 and 800 in 2007, and its new design will lead to a more comprehensive comparative analysis and interpretation of autoinflammatory sequence variants.
AB - Infevers (Internet Fevers; http://fmf.igh.cnrs.fr/ISSAID/infevers), a website dedicated to mutations responsible for hereditary autoinflammatory diseases, was created in 2002 and has continued to evolve. This new version includes eight genes; six were already present: MEFV, MVK, TNFRSF1A, NLRP3, NOD2, PSTPIP1, and two are new, LPIN2 and NLRP7. Currently, Infevers contains over 540 sequence variants. Several new database functions were recently instituted. The website now accepts confidential data and complex alleles. For each gene, a newly created menu offers: 1) a tabular list of the variants that can be sorted by several parameters; 2) a gene graph providing a schematic representation of the variants along the gene; 3) statistical analysis of the data according to the phenotype, alteration type, and location of the mutation in the gene; 4) the cDNA and gDNA sequences of each gene, showing the nucleotide changes along the sequence, with a color-based code highlighting the gene domains, the first ATG, and the termination codon; and 5) a "download" menu making all tables and figures available for the users, which, except for the gene graphs, are all automatically generated and updated upon submission of the variants. Finally, the entire database was curated to comply with the HUGO Gene Nomenclature Committee (HGNC) and HGVS nomenclature guidelines, and wherever necessary, an informative note was provided. Infevers has already proven useful for the scientific community with a mean number of visits per month of 200 in 2002 and 800 in 2007, and its new design will lead to a more comprehensive comparative analysis and interpretation of autoinflammatory sequence variants.
KW - Autoinflammatory disease
KW - Infevers
KW - LPIN2
KW - MEFV
KW - MVK
KW - NLRP3
KW - NLRP7
KW - NOD2
KW - PSTPIP1
KW - Registry
KW - TNFRSF1A
UR - http://www.scopus.com/inward/record.url?scp=44849122715&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=44849122715&partnerID=8YFLogxK
U2 - 10.1002/humu.20720
DO - 10.1002/humu.20720
M3 - Review article
C2 - 18409191
AN - SCOPUS:44849122715
SN - 1059-7794
VL - 29
SP - 803
EP - 808
JO - Human Mutation
JF - Human Mutation
IS - 6
ER -