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中文
这个来自TCPR1503项目的等位基因是在表型基因组学中心通过电穿孔，使用了带有GTCTTCACACGAGACGTAGA指导RNA的Cas9核糖核酸蛋白复合物，目标是关键区域的5'端和CGTGCTCGGTGCTGTTATTC的3'端。这导致了chr7:139516225-139516230的6个碱基插入（6-bp indel）以及chr7:139516241-139516901区域的661个碱基缺失（661-bp del，GRCm38建库）。(J:265051)
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
