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Exon 2 of the gene was flanked by two LoxP sites. Cre-mediated recombination in the germline resulted in the deletion of exon 2. Western blot analysis confirmed the complete absence of protein expression in the hearts of E11.5 homozygous mutant embryos. (J:256653)
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
