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中文
这个来自项目Krt80-6977J-M3128的等位基因是由Jackson实验室通过向细胞注射Cas9 RNA和4个引导序列产生的：ACTTCCTCTTTCTCCACCTT、CACCCCACCAGAGTACAGCC、TGACAGGGAGCCCCACCTCG和AGATGAGCTGCCCTGTGACA。这个变异导致了15号染色体负链101,364,511bp位置起始的378bp缺失，直到101,364,134bp的CTGGTGGGGTGCACCCAAG，位于第3内含子。这个突变删除了exon 2，预测会导致在第101个氨基酸后产生早停。(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
