The Human Gene Mutation Database: 2008 update

被引：650

作者：

Stenson, Peter D. ^{[1
]}

Mort, Matthew ^{[1
]}

Ball, Edward V. ^{[1
]}

Howells, Katy ^{[1
]}

Phillips, Andrew D. ^{[1
]}

Thomas, Nick S. T. ^{[1
]}

Cooper, David N. ^{[1
]}

机构：

[1] Cardiff Univ, Inst Med Genet, Cardiff CF14 4XN, S Glam, Wales

来源：

GENOME MEDICINE | 2009年 / 1卷

关键词：

DISEASE; INFORMATION; PREDICTION; GENOME;

D O I：

10.1186/gm13

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

The Human Gene Mutation Database (HGMD (R)) is a comprehensive core collection of germline mutations in nuclear genes that underlie or are associated with human inherited disease. Here, we summarize the history of the database and its current resources. By December 2008, the database contained over 85,000 different lesions detected in 3,253 different genes, with new entries currently accumulating at a rate exceeding 9,000 per annum. Although originally established for the scientific study of mutational mechanisms in human genes, HGMD has since acquired a much broader utility for researchers, physicians, clinicians and genetic counselors as well as for companies specializing in biopharmaceuticals, bioinformatics and personalized genomics. HGMD was first made publicly available in April 1996, and a collaboration was initiated in 2006 between HGMD and BIOBASE GmbH. This cooperative agreement covers the exclusive worldwide marketing of the most up-to-date (subscription) version of HGMD, HGMD Professional, to academic, clinical and commercial users.

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