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中文
在exon 13的第402位，酪氨酸(Trp, Tyr)被替换为苯丙氨酸(Phenylalanine, Phe)，通过sgRNA和ssODN模板，使用了CRISPR/Cas9技术，这一突变阻止了编码肽中的该残基的自磷酸化。(来源：J:307509)
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
