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中文
CRISPR/Cas9技术用于在exon 2处产生了32bp的缺失。这个等位基因预测会编码一个严重尾端缺失的蛋白质，缺失所有必需的功能区域。从纯合突变小鼠气管组织中提取的cDNA序列分析确认了这个32bp的缺失。RT-qPCR分析显示，来自纯合突变小鼠呼吸道细胞培养物的转录本水平显著降低。(来源：J:274880)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
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 |
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References Literature
Title
PMID
Journal
Year
IF
