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中文
这个来自TCPR1498项目的等位基因是在表型遗传学中心通过电穿孔，使用了带有CTTCCCACTTACCGCCACAC和CAGCTTCGGGTGTCATCGCC这两种特定引物RNA，针对chr8染色体的5'和3'端，生成的。这导致了一个896bp的缺失，位置在8号染色体69793497-69794392（等同于p.E130Gfs*1，GRCm38建库）。(引用：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
