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中文
这个突变是在Jackson实验室通过电穿孔Cas9蛋白和指导序列TGCAGAATTGAAGATCCAGT和CCATGACAGTGATATCATCC产生，导致了从8号染色体105,320,175bp起始，至105,321,684bp后终止的1510bp缺失(参考GRCm39/mm39基因组).这个变异删除了ENSMUSE00000334359(第2外显子)的1510bp，并预测会导致第7位氨基酸序列改变以及随后的第41位终止。(来源：J:188991)
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
