Genome cross-referencing and XREFdb: Implications for the identification and analysis of genes mutated in human disease

被引:68
作者
Bassett, DE
Boguski, MS
Spencer, F
Reeves, R
Kim, SH
Weaver, T
Hieter, P
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT MOL BIOL & GENET,BALTIMORE,MD 21205
[2] JOHNS HOPKINS UNIV,SCH MED,CTR GENET MED,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV,SCH MED,DEPT PHYSIOL,BALTIMORE,MD 21205
[4] NATL LIB MED,NATL CTR BIOTECHNOL INFORMAT,NIH,BETHESDA,MD 20894
关键词
HOMOLOG; ENCODES; CANCER;
D O I
10.1038/ng0497-339
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Comparative genomics approaches and multi-organismal biology are valuable tools for genetic analysis. Cross-species connections between genes mutated in human disease states and homologues in model organisms can be particularly powerful, as model-organism gene function data and experimental approaches can shed light an the molecular mechanisms defective in the disease. We describe a project that is systematically identifying novel expressed sequence tag (EST) sequences that are highly related to genes in model organisms and mapping them to positions on the mouse and human maps. This process effectively cross-references model organism genes with mapped mammalian phenotypes, facilitating the identification of genes mutated in human disease states via the positional candidate approach. A public database, XREFdb (http://www.ncbi.nlm.nih.gov/XREFdb/), disseminates similarity search, mapping and mammalian phenotype information and increases the rate at which these cross-species connections are established.
引用
收藏
页码:339 / 344
页数:6
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