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中文
这个来自TCPR0432项目的研究等位基因是在phenogenomics中心通过向细胞注射Cas9 mRNA和四种引导RNA，这些RNA带有TCCTGTGACATTGCGTTTAC和CTGGACAGTACTGATCTGGA的 spacer序列，目标是ENSMUSE00001228124(第5外显子，即exon 5)的5'端，以及GCCACGCCATGCTTAGGTCT和GGTAGGATGCTCCCACTCGG的3'端。这导致了chr11染色体上一个316bp的缺失，从97,666,855到97,667,000，同时插入了19bp的GACGCCACGCCATGCTTAG。(参考GRCm38，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
