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中文
从exon 1到3区域被标记了。通过cre介导的重组，删除了位于exon 3下游的含荧光素的诺卡因抗性基因座。一个点突变导致了第114位氨基酸由Alanine替换为Arginine（R114A）。 Western blot结果显示，这种严重发育不良等位基因的蛋白水平减少了大约80%到90%。（来源：J:204811）
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
