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中文
CRISPR/Cas9技术在exon 2的第101位氨基酸由lysine替换为alanine（KR变为AA），第102位氨基酸由arginine替换为alanine（KR变为AA）。这种AA突变破坏了Vax1的GAG糖结合位点，产生了一种从视神经管细胞到视神经节轴突传递缺陷的蛋白质。（来源：J:333797）
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
