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中文
这个来自TCPR0676项目的等位基因是在phenogenomics中心通过向细胞注射Cas9 mRNA和三个指导RNA，这些RNA带有AGCAAGTTGTATTCCCCTGC和CGCCCCGATGCACCAATTAC的 spacer序列，目标是ENSMUSE00000842756和ENSMUSE00001286785基因的5'端和3'端。这导致了chrX染色体上一个2915bp的缺失，位置从95,922,379到95,925,293（GRCm38参考）。(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
