Exon 4 was targeted by introduction of TALEN mRNA into fertilized B6.Cg-Fcgrttm1Dcr Tg(FCGRT)32Dcr/DcrJ oocytes and the resulting founder screened and found to have a 2 base pair deletion beginning at Chromosome 5 base 90,464,113 (GRCm38.p2) which is predicted to result in a frame shift then a premature stop codon 5 amino acids downstream of the encoded frame shift. By ELISA, heterozgyotes have a decrease in serum albumin of approximately 30 percent and homozygotes have no detectable serum albumin. (J:220803)
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模型ID
品系来源
等位基因类型
突变
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B6.Cg-Fcgrttm1Dcr Tg(FCGRT)32Dcr/DcrJ
Endonuclease-mediated
Intragenic deletion
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1
5
3

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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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