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中文
在ENSMUST00000047321的exon 5中，serine的42位(AGT)被替换为alanine( GCC)，通过sgRNA(靶向GTGTGGACTGCAATCGCAAG)和ssODN模板，应用了CRISPR/Cas9技术。这个突变导致编码肽中的受累氨基酸无法被磷酸化。(来源：J:342247)
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
