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中文
在exon 16中的核苷酸替换导致了第702位的氨基酸由 cysteine 替换为 arginine（R702C）。通过Cre介导的重组，去除了位于exon 15上游的含荧光素的诺卡因抗性基因座。(来源：J:204923)
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
