GENETICS OF SLEEK - POSSIBLE REGULATORY MUTATION OF THE TABBY-CRINKLED-DOWNLESS SYNDROME

被引:13
作者
CROCKER, M
CATTANACH, BM
机构
[1] MRC Radiobiology Unit, Harwell, Oxon
关键词
D O I
10.1017/S0016672300019479
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A new mutation, Sleek, similar in appearance to mutations at the Ta, cr and dl loci, has been investigated. It is inherited as an autosomal dominant and maps very close to dl on chromosome 13. Allelism with dl seems probable since Sleek interacts with dl but not with cr. The unusual occurrence of dominant and recessive alleles at the same locus which produce a similar mutant phenotype suggests that the locus might either code for a multimeric protein or a regulatory product. © 1979, Cambridge University Press. All rights reserved.
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页码:231 / 238
页数:8
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