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The IARC TP53 Mutation Database compiles all TP53 gene variations identified
in human populations and tumor samples. Data are compiled from the peer-reviewed literature and from generalist databases.
The following datasets are available:
TP53 somatic mutations in sporadic cancers
TP53 germline mutation in familial cancers
Common TP53 polymorphisms identified in human populations
Functional and structural properties of P53 mutant proteins
TP53 gene status in human cell-lines
Mouse-models with engineered TP53
The database includes various annotations on the predicted or experimentally assessed functional impact of mutations,
clinicopathologic characteristics of tumors and demographic and life-style information on patients.
The database is meant to be a source of information on TP53 mutations for a broad range of scientists and clinicians who work in different research areas:
Basic research, to study the structural and functional aspects of the p53 protein
Molecular pathology of cancer, to understand the clinical significance of mutations identified in cancer patients
Molecular epidemiology of cancer, to analyze the links between specific exposures and mutation patterns and to make inferences about possible causes of cancer
Molecular genetics, to analyze genotype/phenotype relationships
See detailed information on database contents in the user's guide.
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 The database has been updated in december 2009: the current release is R14. Check what's new here.
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Report on the p53 MARATHON 2009 held in Acre, Israel, this March, here
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The 15th International p53 Workshop will be held in Philadelphia, October 8—12, 2010 (mailing list: rjen at mail.med.upenn.edu.)
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When using the database, authors should cite the following publication:
Petitjean A, Mathe E, Kato S, Ishioka C, Tavtigian SV, Hainaut P, Olivier M.
Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 database. Hum Mutat. 2007 Jun;28(6):622-9.
The version of the database should be identified (R14, November 2009 is the latest).
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©2009 International Agency for Research on Cancer - All Rights Reserved.
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