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The floxed exon in Llglhtm1Vv was removed via cre-mediated recombination, leaving a single LoxP site in its place. The deletion resulted in a frame shift in translation of the protein, which is predicted to disrupt translation after the first 27 amino acids that do not encode any known domains. Western blot analysis from mutants showed no protein was present. (J:89028)
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
