Point mutations were introduced into the gene that altered codon 286 from one encoding threonine to one encoding alanine. This mutation had been shown in vitro to eliminate autophosphorylation at this site and result in the elimination of calcium-calmodulin independent activity without affecting calcium-calmodulin dependent activity. An adjacent loxP-flanked neomycin cassette was removed by transient Cre mediated recombination in ES cells prior to the production of chimeric mice. Western blot and immunohistochemistry experiments on homozygous mice confirmed that a stable mutant protein was produced from this allele. (J:45750)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
(129X1/SvJ x 129S1/Sv)F1-Kitl+
Targeted
Insertion, Nucleotide substitutions
--
1
3
36

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

References Literature

Title
PMID
Journal
Year
IF
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