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This allele resulted from loss of the 3' loxP site from Epc1tm1a(EUCOMM)Wtsi, a "KO first" allele having a frt site-flanked splice acceptor-lacZ/neo-pA cassette followed by a loxP site upstream of exon 2 and a second loxP site downstream of exon 2. The present allele cannot be converted to a conditional allele. (J:173534)
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
