The CDKN2A database: Integrating allelic variants with evolution, structure, function, and disease association

被引:24
作者
Murphy, JA
Barrantes-Reynolds, R
Kocherlakota, R
Bond, JP
Greenblatt, MS
机构
[1] Univ Vermont, Vermont Canc Ctr, Burlington, VT 05401 USA
[2] Univ Vermont, Dept Med, Burlington, VT 05401 USA
[3] Univ Vermont, Dept Microbiol & Mol Genet, Burlington, VT 05401 USA
关键词
mutation; somatic; germline; familial melanoma; cell cycle; tumor suppressor gene; p16; Ink4a; ARF; curation;
D O I
10.1002/humu.20083
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In this report, we introduce the CDKN2A Database, an online database of germline and somatic variants of the CDKN2A tumor suppressor gene recorded in human disease through the year 2002, annotated with evolutionary, structural, and functional information. The CDKN2A Database improves upon existing resources by: 1) including both somatic mutations and germline variants, thereby adding the perspective of somatic cell carcinogenesis to that of hereditary cancer predisposition; 2) including information that assists with the interpretation of allelic variants, such as other primary data (sequences, structures, alignments, functional measurements, and literature references) and annotations (extensive text, figures, and a tree-based phylogenetic classification); and 3) providing the information in a format that allows a user to either download the database or to easily manipulate it online. We describe the database structure, content, current uses, and potential implications (http://biodesktop.uvm.edu/perl/p16). (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:296 / 304
页数:9
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