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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
基因编辑小鼠
P2rx7
tm1.1(P2RX7)Jde
Alias:
P2rx7
hP2RX7
P2rx7
hWT
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基础信息
表型特征
文献报道
这个靶向载体从5'到3'的构建如下:一个loxP位点后面跟着小鼠内皮1的3'端(1.4kb); 小鼠的第二个外显子被替换为人P2RX7基因的cDNA,包括2-13号exons; 一个反向定向的筛选标记,由frt座点 flank,包含磷酸二羟丙酮酸激酶(PGK)驱动的诺卡因抗性基因,带有牛生长激素(bGH)的poly A信号(pA),第二个loxP位点,以及一个由bGHpA、PGK pA和2个SV40 pAs组成的四重poly A序列。通过在ES细胞中通过同源重组传递修改后的等位基因后,来自雄性杂交后代的后代会被繁殖。通过与删除者-flp小鼠杂交,FRT座点周围的neo cassette会被剔除。(来源:J:244726)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
6203041
129S2/SvPas
Targeted
Insertion, Intergenic deletion
--
1
1
4
Phenotypes
Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes
References Literature
Title
PMID
Journal
Year
IF
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