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中文
在49号 arginine位置，通过同源重组被替换成了 cysteine。插入了位于1号和2号外显子之间的 loxP 包围的诺卡因基因座。蛋白表达量的降低通过色谱图得到了确认（在杂合子小鼠的晶状体中减少了30%）。（来源：J:132296）
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
