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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Map2k1
mitogen-activated protein kinase kinase 1
MGI:1346866
37 phenotypes from 8 alleles in 14 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Map2k1em1(IMPC)H/Map2k1em1(IMPC)H
C57BL/6NTac-Map2k1em1(IMPC)H/H
preweaning lethality, complete penetrance J:211773
Map2k1Gt(ROSABetageo)J2Chrn/Map2k1Gt(ROSABetageo)J2Chrn
involves: 129/Sv * 129S/SvEv * C57BL/6J * SJL
abnormal angiogenesis J:54197
abnormal cell migration J:54197
abnormal placenta labyrinth morphology J:54197
abnormal placental labyrinth vasculature morphology J:54197
abnormal spongiotrophoblast layer morphology J:54197
abnormal vascular endothelial cell migration J:54197
decreased embryo size J:54197
embryo tissue necrosis J:54197
embryonic lethality during organogenesis, incomplete penetrance J:54197
pale yolk sac J:54197
Map2k1Gt(ROSABetageo)J2Chrn/Map2k1Gt(ROSABetageo)J2Chrn
involves: 129/Sv * C57BL/6J * SJL
abnormal placenta labyrinth morphology J:112223
abnormal placenta morphology J:112223
embryonic lethality during organogenesis, complete penetrance J:112223
small placenta J:112223
Map2k1tm1.1Bacc/Map2k1tm1.1Bacc
129-Map2k1tm1.1Bacc
embryonic lethality during organogenesis, complete penetrance J:199705
Map2k1tm1.1Bacc/Map2k1tm1.1Bacc
either: 129-Map2k1tm1.1Bacc or (involves: 129P2/OlaHsd * C57BL/6)
abnormal trophoblast layer morphology J:199705
absent ectoplacental cone J:199705
Map2k1tm1.1Bacc/Map2k1tm1.1Bacc
involves: 129P2/OlaHsd * C57BL/6
embryonic lethality during organogenesis, complete penetrance J:199705
Map2k1tm1.1Chrn/Map2k1tm1.1Chrn
involves: 129S/SvEv * FVB/N
embryonic lethality during organogenesis, complete penetrance J:112223
Map2k1tm1Bacc/Map2k1tm1.1Bacc
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129P2/OlaHsd * C57BL/6 * CBA
no abnormal phenotype detected J:199705
Map2k1tm1Bacc/Map2k1tm1.1Bacc
Meox2tm1(cre)Sor/Meox2+
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6
normal mortality/aging J:199705
Map2k1tm1Bacc/Map2k1tm1.1Bacc
Tg(Nes-cre)1Kln/0
involves: 129P2/OlaHsd * C57BL/6 * SJL
normal nervous system phenotype J:199705
postnatal growth retardation J:199705
Map2k1tm1Chrn/Map2k1tm1.1Chrn
Edil3Tg(Sox2-cre)1Amc/?
involves: 129S/SvEv * C57BL/6 * CBA * FVB/N
normal reproductive system phenotype J:112223
Map2k1tm2.1Chrn/Map2k1+
involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL/J
pulmonary artery stenosis J:261678
Map2k1tm2.1Chrn/Map2k1tm1.1Chrn
involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL/J
decreased cranium length J:261678
decreased cranium width J:261678
increased inner canthal distance J:261678
pulmonary artery stenosis J:261678
Map2k1tm2.1Chrn/Map2k1tm2.1Chrn
involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL/J
increased astrocyte number J:261678
increased cranium length J:261678
increased oligodendrocyte number J:261678
pulmonary artery stenosis J:261678
Tg(Myh6-Map2k1*)1Jmol/?
involves: FVB
decreased cardiomyocyte apoptosis J:66102
decreased left ventricle diastolic pressure J:66102
heart left ventricle hypertrophy J:66102
increased heart weight J:66102
increased left ventricle systolic pressure J:66102
increased myocardial fiber size J:66102
thick ventricular wall J:66102
Tg(Myh6-Map2k1*)1Jmol/?
involves: FVB/N
abnormal cardiac output J:127872
decreased cardiomyocyte apoptosis J:127872
decreased myocardial infarct size J:127872

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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
04/16/2024
MGI 6.23
The Jackson Laboratory