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中文
这个来自TCPR0855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TGTGCACGAAATCTACAGTG、TAATCCAGGGGCAGTGCCAA和CCGAACCAGCACCACTGGTG间隔序列的Cas9核糖核酸蛋白复合物，产生的。这导致了16个碱基的删除，位置在chr11:60865301至60865316，具体变异为_TGCACGAAATCTACAG; c.89_104缺失(TGCACGAAATCTACAG);以及p.H31G*fs23（GRCm38建库）。(引用信息：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
