首页> 外文OA文献 >Updated catalogue of homologues to human disease-related proteins in the yeast genome1Notation: nucleotide and protein sequences identifiers are given as DATABASE:IDENTIFIER where the codes for the corresponding data bases are SW (for SwissProt), EMBL, TREMBL, SPTREMBL, PIR, and OMIM. The corresponding sequences can be retrieved through the web using SRS (T. Etzold, http://www.ebi.ac.uk/srs/srsc), and the OMIM data base (B. Brylawski, http://www.ncbi.nlm.nih.gov/Omim/). All yeast sequences are tagged by their MIPS gene identifier (Yxynnnz, where x indicates chromosome, y stands for the arm, nnn is a numeral, and z indicates the direction of translation).1

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Updated catalogue of homologues to human disease-related proteins in the yeast genome1Notation: nucleotide and protein sequences identifiers are given as DATABASE:IDENTIFIER where the codes for the corresponding data bases are SW (for SwissProt), EMBL, TREMBL, SPTREMBL, PIR, and OMIM. The corresponding sequences can be retrieved through the web using SRS (T. Etzold, http://www.ebi.ac.uk/srs/srsc), and the OMIM data base (B. Brylawski, http://www.ncbi.nlm.nih.gov/Omim/). All yeast sequences are tagged by their MIPS gene identifier (Yxynnnz, where x indicates chromosome, y stands for the arm, nnn is a numeral, and z indicates the direction of translation).1

机译：酵母基因组中与人类疾病相关的蛋白质的同源物更新目录1注释：核苷酸和蛋白质序列的标识符以DATABASE：IDENTIFIER给出，其中相应数据库的代码为SW（SwissProt），EMBL，TREMBL，SPTREMBL，PIR和OMIM。可以使用SRS（T。Etzold，http：//www.ebi.ac.uk/srs/srsc）和OMIM数据库（B. Brylawski，http：//www.ncbi）通过网络检索相应的序列。 .nlm.nih.gov / Omim /）。所有酵母序列均通过其MIPS基因标识符进行标记（Yxynnnz，其中x表示染色体，y表示臂，nnn是数字，z表示翻译方向）。1

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Andrade Miguel A; Sander Chris; Valencia Alfonso;
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年度 1998
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1. Three novel types of splicing aberrations in the tuberous sclerosis TSC2 gene caused by mutations apart from splice consensus sequences11Accession numbers and URLs for data in this article are as follows: Online Mendelian Inheritance in Man: http://www.ncbi.nlm.nih.gov/omim. For TSC1 (MIM 191100) and TSC2 (MIM 191092). The Human Gene Mutation Data Base, Cardiff (HGMD): http://www.uwcm.acuk/uwcm/mg. For TSC1 120735 and for TSC2 120466. TSC Variation Database: http://www.expmed.bwh.harvard.edu/projects/tsc_database. GenBank: http://www.ncbi.nlm.nih.gov/Genbank. For TSC2 cDNA X75621 and TSC2 complete genomic sequence AC005600. [O] . Mayer Karin, Ballhausen Wolfgang, Leistner Werner, 2000

机译：除剪接共有序列外，由突变引起的结节性硬化性TSC2基因中的三种新型剪接畸变11本文的登录号和URL如下：Man的在线孟德尔遗传：http：//www.ncbi.nlm.nih。 gov / omim。用于TSC1（MIM 191100）和TSC2（MIM 191092）。人类基因突变数据库，加的夫（HGMD）：http：//www.uwcm.acuk/uwcm/mg。对于TSC1 120735和TSC2120466。TSC变更数据库：http://www.expmed.bwh.harvard.edu/projects/tsc_database。 GenBank：http：//www.ncbi.nlm.nih.gov/Genbank。对于TSC2 cDNA X75621和TSC2，完整的基因组序列AC005600。

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