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中文
在1C外显子和1B外显子之间，以及一个由弗里特(frt)序列标记的氨苄西林抗性插入下游的2号内含子中插入了LoxP位点。1B到2号外显子被标记为可删除。这个突变体被用来产生Ptch1tm1Cklr（J:159972）。
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
