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中文
在exon 12内引入了一个单核苷酸变异，导致了K661R的氨基酸替换，并通过同源重组在intron 11内插入了一个可删除的诺卡因磷酸转移酶基因座。这一改变预计会干扰激酶活性。选择性基因座已通过Cre介导的重组移除。(来源：J:157019)
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
