ENU mutagenesis of mice carrying the Mpltm1Wsa allele caused a C-to-A mutation in the 25th nucleotide pair of exon 12. This mutation is predicted to cause the substitution of a lysine for a threonine at residue 429 in the highly conserved Src activation loop of the protein product. Founder mice were bred with wild-type mice to breed away the Mpltm1Wsa allele. Mutant protein isolated from the B cells of homozygous mice was found to lack kinase activity in an in vitro transkinase assay. (J:144799)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
B6.129S1-Mpltm1Wsa
Chemically induced
Single point
--
1
1
2

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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