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中文
一段1.9千碱基对的基因片段被诺卡因抗性基因座的插入所打断。exon 2（包含ATP结合位点）和内含子2/3的5'切割位点发生了移位，导致它们失去了原有的阅读框。多组织 Western blot 实验在纯合无基因突变小鼠的所有组织中都确认了该基因的功能缺失。 (Source: None)
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
