The mutant mouse line yeti was isolated in a recessive ENU mutagenesis screen for genes affecting embryonic development. The locus was mapped to a 3.5 Mb interval between rs6278243 and rs29154438 on chromosome 12. A single G>A mutation was identified in the splice acceptor site of exon 22. RT-PCR analysis of cDNA confirmed aberrant splicing of the Wdr35 mRNA in heterozygous and homozygous embryos. Sequencing of these mutant splice variants revealed frameshifts in all transcripts. Noncomplementation of this allele with an embryonic stem cell derived targeted null allele proves that the mutant phenotype is due to this point mutation. (J:171617)
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基础信息

模型ID
品系来源
等位基因类型
突变
遗传方式
相关基因
相关疾病
参考文献
Not Specified
Chemically induced
Single point
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1
6
2

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标签摘要:
hm: 纯合子
ht: 杂合子
cn: 条件基因型
cx: 复合型:涉及多基因组
tg: 转基因
ot: 其他:半合子、不确定...
(F): 雌性
(M): 雄性
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N: 正常表型
(#): 上标括号内为相关疾病数量
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