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中文
CRISPR/Cas9介导的突变产生了一个15个碱基的内含子附近5'端的15bp缺失，导致5个氨基酸（GPQFPFKGVDDRESW）的缺失，以及一个3个碱基的内含子缺失，造成第244位的Thr（Thr）缺失。(来源：J:248812)
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
