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A 2.9 kb genomic fragment extending from within intron 2 through exon 3 was replaced with a single loxP site. The deleted region encompassed 0.26 kb of intron 2, the entire open reading frame of exon 3, the 3' non-coding region of exon 3, and 0.6 kb of adjacent 3' sequence. (J:67593)
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
