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A construct with the human skeletal alpha actin promoter driving the mouse calpain 3 sequence lacking exon 15, thereby removing the IS2 domain, was microinjected into (C57BL/6J x BALB/c)F2 oocytes and integrated via random insertion. (J:77348)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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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References Literature
Title
PMID
Journal
Year
IF
