移码突变
错义突变
生物
遗传学
遗传性多发性外生骨疣
基因
无义突变
胡说
突变
分子生物学
出处
期刊:Human Mutation
[Wiley]
日期:2000-03-01
卷期号:15 (3): 220-227
被引量:198
标识
DOI:10.1002/(sici)1098-1004(200003)15:3<220::aid-humu2>3.0.co;2-k
摘要
Hereditary multiple exostoses (EXT) is an autosomal dominant disorder characterized by the formation of exostoses, which are cartilage-capped bony protuberances mainly located on long bones. Two genes, EXT1 and EXT2, and at least one other unidentified gene, are known to be involved in the formation of exostoses. To date, 49 different EXT1 and 25 different EXT2 mutations have been found in EXT patients, and there is evidence that mutations in these two genes are responsible for over 70% of the EXT cases. Among the 49 EXT1 mutations there are 9 nonsense, 21 frameshift, and 5 splice site mutations; 2 in-frame deletions of 1 and 5 amino acids respectively; and 12 missense mutations. For EXT2, 8 nonsense, 11 frameshift, 3 splice site and 3 missense mutations are described. The majority of these mutations are mutations causing loss of function, which is consistent with the presumed tumor suppressor function of the EXT genes.
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