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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Map2k5tm1Ctr
targeted mutation 1, Cathy Tournier
MGI:3526901
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Map2k5tm1Ctr/Map2k5tm1Ctr involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3527216
ht2
Map2k5tm1Ctr/Map2k5+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3527217


Genotype
MGI:3527216
hm1
Allelic
Composition
Map2k5tm1Ctr/Map2k5tm1Ctr
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map2k5tm1Ctr mutation (0 available); any Map2k5 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygotes die at approximately E10.5, with no homozygotes found at E11.5

cardiovascular system
• trabeculation of the bulbus cordis and the common ventricular chamber is highly disorganized at E10.5
• the spiral septum of the outflow tract displays little or no septal development at E10.5
• E10.5 homozygotes exhibit abnormal heart development
• little evidence of the formation of the endocardial cushion tissue in the atroventricular canal

cellular
• the head, heart and dorsal regions of E10.5 embryos exhibit an increase in apoptosis, with increased apoptosis observed as early as E9.5
• the head, heart, and dorsal regions of E10.5 embryos exhibit a decrease in cell proliferation, however observe no effect on cell cycle progression

embryo
• severely retarded growth especially of the heart, head and limbs

growth/size/body

muscle
• trabeculation of the bulbus cordis and the common ventricular chamber is highly disorganized at E10.5




Genotype
MGI:3527217
ht2
Allelic
Composition
Map2k5tm1Ctr/Map2k5+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map2k5tm1Ctr mutation (0 available); any Map2k5 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• heterozygous mutants appear healthy and fertile





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory