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A single loxP site was left in place of exon 1 after the insertion and subsequent removal of a floxed neo cassette by homologous recombination and in vitro cre mediated excision. The deleted region encoded the start codon as well as the PP1 and glycogen-binding domains. Western blot analysis of homozygous mutant skeletal muscle indicated an absence of protein. (J:82422)
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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References Literature
Title
PMID
Journal
Year
IF
