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中文
Exon 4被替换为人类的Exon 4，它代表p.R72P单核苷酸变异（SNP rs1042522）中的arginine变异型。上游的诺卡因抗性基因座，由loxP位点引导，通过Cre介导的重组已被去除。（来源：J:162466）
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
