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Phenotypes Associated with This Genotype
Genotype
MGI:5288513
Allelic
Composition
Mapk11tm1Jsca/Mapk11tm1Jsca
Mapk14tm2Nbr/Mapk14tm3.1(Mapk11)Nbr
Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Edil3Tg(Sox2-cre)1Amc mutation (5 available); any Edil3 mutation (43 available)
Mapk11tm1Jsca mutation (0 available); any Mapk11 mutation (31 available)
Mapk14tm2Nbr mutation (2 available); any Mapk14 mutation (43 available)
Mapk14tm3.1(Mapk11)Nbr mutation (0 available); any Mapk14 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Cardiac defects in Mapk14tm3.1(Mapk11)Nbr/Mapk14tm2Nbr Edil3Tg(Sox2-cre)1Amc/0 Mapk11tm1Jsca/Mapk11tm1Jsca embryos

mortality/aging
• present in the expected numbers at E18.5 but none are found at weaning

cardiovascular system

nervous system
N
• spina bifida phenotype seen in double null mice is rescued in mice carrying the Mapk14tm3.1(Mapk11)Nbr allele


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/25/2025
MGI 6.24
The Jackson Laboratory