A 53bp segment of DNA containing the intron 2 5-prime splice site of endogenous mouse Sbds was replaced with 50 bp containing the intron 2 5-prime splice site found in human shwachman-diamond syndrome patients, c.258+2T>C. Assessment in MEFs shows that this is a hypomorph with aberrant splicing from a cryptic exon 2 splice site, and exon 2 skipping, with the residual wild type expression less than that found in the human samples. (J:335832)
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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
C57BL/6J
Endonuclease-mediated
Insertion, Intragenic deletion, Nucleotide substitutions
Not Specified
1
8
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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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