CRISPR/cas9 methodologies are used to introduce an H170N (nucleotide change CAC to AAT, note AAC was originally reported) in exon 2. The mutation disrupts interactions between FLRT2 and its ligands UNC5C and UNC5D. A single guide RNA (sgRNA) was produced in which the PAM sequence overlaps the H170 codon (sequence 5' GCCCAACAGGCACGCTACTCagg; PAM site is denoted by lowercase letters). The PAM sequence is destroyed by the codon-altering mutation, thereby rendering correctly edited alleles immune to further cas9 cutting activity. (J:339867)
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基础信息

模型ID
品系来源
等位基因类型
突变
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相关基因
相关疾病
参考文献
(C57BL/6 x SJL)F1
Endonuclease-mediated
Nucleotide substitutions
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1
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1

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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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