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中文
CRISPR/Cas9技术在距离起始翻译位点+49,561到+49,584的exon 7上产生了一个24个碱基的内含子缺失。这个缺失导致exon 7的跳过，并产生了exon 6到exon 8的替代剪接，从而产生野生型的Nfix等位基因。MEFs细胞中表达的是突变的长等位基因(293bp)和缺失exon 7的野生型短等位基因(194bp)。(来源：J:343087)
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
