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来自项目Mrgprg-115062J-8267M的这个等位基因是在Jackson实验室通过电穿孔Cas9蛋白和两个引导序列ATAGCCCCCCAAGACCTGAC和TGTTCTCCATATTCAACATC产生的，导致了7号染色体143,764,544bp到143,765,362bp（GRCm38/mm10）位置的819bp缺失。这个变异删除了ENSMUSE00000378852（第2外显子）的819bp，预测会导致从第4位到第277位氨基酸序列缺失273个。这将几乎移除编码序列的全部，只剩下16个氨基酸。(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
