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中文
这个等位基因来自TCPR0433项目，由中心性表观基因组学通过向细胞注入Cas9 mRNA和两组指导RNA（含spacer序列：GTTCGATCCTCGCTGGCCAG, CGCTACCAGGTGTTCTTCTT, GCGGTCCAGGGCCTGATTGT, TCTACAAACACCGTGACTAC）产生，导致了168个碱基在chr13上从26,769,233到26,770,021的位置缺失（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
