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中文
这个来自TCPR0949项目的研究等位基因是在phenogenomics中心通过电穿孔，使用ATACCATCCTACACCAGACT和AGGAATGGATCAATCCACGC的单链RNA指导元件，针对基因ENSMUSE00000602528和ENSMUSE00000602527的5'端，以及TGATTCAACTTTAAAGACGG和GGAGAACAAGTCAGTGACGA针对3'端，产生了838bp的缺失。变异位置在chr1:52640706到52641543，参照GRCm38建库(来源：J:200814)
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
