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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mapk14tm1Mka
targeted mutation 1, Michael Karin
MGI:2177830
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Mapk14tm1Mka/Mapk14tm1Mka involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:2177932
ht2
Mapk14tm1Mka/Mapk14+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:3663735


Genotype
MGI:2177932
hm1
Allelic
Composition
Mapk14tm1Mka/Mapk14tm1Mka
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mapk14tm1Mka mutation (1 available); any Mapk14 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• a significant portion of homozygotes survive to E16.5; however, no live homozygotes are recovered at E18.5
• a portion of homozygotes die between E11.5 and E12.5, probably due to a placental defect
• Background Sensitivity: the frequency of live homozygotes developing after E11.5 is markedly reduced upon backcrossing into the C57BL/6J background

hematopoietic system
• at E11.5 or later, live homozygotes exhibit a severe block of erythroid differentiation in fetal liver, indicating defective definitive erythropoiesis, whereas embryonic erythropoiesis remains unaffected
• failure of definitive erythropoiesis is caused by diminished erythropoietin gene expression
• however, mutant fetal livers contain BFU-Es and CFU-Es at normal frequencies, reconstitute erythropoiesis in lethally irradiated hosts, and undergo terminal differentiation in vitro in the presence of exogenous erythropoietin
• homozygotes that survive up to E16.5 are highly anemic

liver/biliary system
• at E11.5 or later, live homozygotes exhibit small fetal livers
• at E11.5 or later, live homozygotes exhibit pale fetal livers

embryo
• homozygotes that die at E11.5 display a sigificant reduction of embryo-derived blood vessels in the placental labyrinth layer
• some of the homozygotes that die between E11.5 and E12.5 appear growth-retarded
• in contrast, homozygotes that survive beyond E12.5 exhibit normal growth and morphology
• at E11.5 or later, live homozygotes display normal-sized yolk sacs with only a few circulating red blood cells

growth/size/body
• some of the homozygotes that die between E11.5 and E12.5 appear growth-retarded
• in contrast, homozygotes that survive beyond E12.5 exhibit normal growth and morphology

integument
• homozygotes that survive past E12.5 exhibit a slight pallor

cardiovascular system
• homozygotes that die at E11.5 display a sigificant reduction of embryo-derived blood vessels in the placental labyrinth layer




Genotype
MGI:3663735
ht2
Allelic
Composition
Mapk14tm1Mka/Mapk14+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mapk14tm1Mka mutation (1 available); any Mapk14 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• heterozygotes are viable and overtly normal, with no significant differences in heart and body weights or baseline cardiac functional parameters relative to wild-type mice
• however, heterozygotes undergo significantly attenuated ischemia-reperfusion myocardial injury relative to wild-type counterparts
• following ischemia-reperfusion, heterozygotes display a significantly reduced myocardial infarct size relative to wild-type mice (7.20.7% vs 37.12.7%, respectively)

homeostasis/metabolism
• heterozygotes are viable and overtly normal, with no significant differences in heart and body weights or baseline cardiac functional parameters relative to wild-type mice
• however, heterozygotes undergo significantly attenuated ischemia-reperfusion myocardial injury relative to wild-type counterparts
• following ischemia-reperfusion, heterozygotes display a significantly reduced myocardial infarct size relative to wild-type mice (7.20.7% vs 37.12.7%, respectively)





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
12/10/2024
MGI 6.24
The Jackson Laboratory