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雄激素受体基因突变数据库:2012 年更新。

The androgen receptor gene mutations database: 2012 update.

机构信息

Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Quebec, Canada.

出版信息

Hum Mutat. 2012 May;33(5):887-94. doi: 10.1002/humu.22046. Epub 2012 Mar 13.

DOI:10.1002/humu.22046
PMID:22334387
Abstract

The current version of the androgen receptor gene (AR) mutations database is described. A major change to the database is that the nomenclature and numbering scheme now conforms to all Human Genome Variation Society norms. The total number of reported mutations has risen from 605 to 1,029 since 2004. The database now contains a number of mutations that are associated with prostate cancer (CaP) treatment regimens, while the number of AR mutations found in CaP tissues has more than doubled from 76 to 159. In addition, in a number of androgen insensitivity syndrome (AIS) and CaP cases, multiple mutations have been found within the same tissue samples. For the first time, we report on a disconnect within the AIS phenotype-genotype relationship among our own patient database, in that over 40% of our patients with a classic complete AIS or partial AIS phenotypes did not appear to have a mutation in their AR gene. The implications of this phenomenon on future locus-specific mutation database (LSDB) development are discussed, together with the concept that mutations can be associated with both loss- and gain-of-function, and the effect of multiple AR mutations within individuals. The database is available on the internet (http://androgendb.mcgill.ca), and a web-based LSDB with the variants using the Leiden Open Variation Database platform is available at http://www.lovd.nl/AR.

摘要

描述了当前版本的雄激素受体基因 (AR) 突变数据库。数据库的一个主要变化是,命名法和编号方案现在符合所有人类基因组变异协会的规范。自 2004 年以来,报告的突变总数从 605 个增加到 1029 个。该数据库现在包含了一些与前列腺癌 (CaP) 治疗方案相关的突变,而在 CaP 组织中发现的 AR 突变数量从 76 个增加到 159 个以上。此外,在一些雄激素不敏感综合征 (AIS) 和 CaP 病例中,同一组织样本中发现了多个突变。我们首次报告了我们自己的患者数据库中 AIS 表型-基因型关系的不一致性,即我们超过 40%的具有经典完全 AIS 或部分 AIS 表型的患者似乎没有他们的 AR 基因中的突变。讨论了这种现象对未来特定基因座突变数据库 (LSDB) 发展的影响,以及突变可以与功能丧失和获得相关的概念,以及个体中多个 AR 突变的影响。该数据库可在互联网上获得 (http://androgendb.mcgill.ca),并且使用莱顿开放变异数据库平台的变体的基于网络的 LSDB 可在 http://www.lovd.nl/AR 上获得。

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