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中文
这个来自TCPR0782项目的等位基因是在phenogenomics中心通过电穿孔，使用了具有GCGGCCGCGTGGGCCTCAAT和ATCGGGTCTGGCACCGCTCC序列的单导RNA，针对ENSMUSE00000593055基因的5'端，以及TTTCCCTCTCGCAACTGCAC和GAGCCAACGGTCATCAGAGA针对3'端的，产生了chr7染色体上一个1,548bp的缺失，位置从62,418,469到62,420,016（GRCm38建库）。(引用：J:237616)
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
