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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Map2k1tm2.1Chrn
targeted mutation 2.1, M Jean Charron
MGI:6157680
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Map2k1tm2.1Chrn/Map2k1tm2.1Chrn involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL/J MGI:6159581
ht2
Map2k1tm2.1Chrn/Map2k1+ involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL/J MGI:6159580
ht3
Map2k1tm2.1Chrn/Map2k1tm1.1Chrn involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL/J MGI:6159582


Genotype
MGI:6159581
hm1
Allelic
Composition
Map2k1tm2.1Chrn/Map2k1tm2.1Chrn
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map2k1tm2.1Chrn mutation (1 available); any Map2k1 mutation (92 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• pulmonary artery stenosis is observed at E13.5
• left and right pulmonary artery lumen areas are reduced

craniofacial

nervous system
• increased density of GFAP+ astrocytes is found in sensory cortices and hippocampal CA1
• increased density of oligodendrocytes in the sensory cortex

skeleton

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cardiofaciocutaneous syndrome DOID:0060233 OMIM:PS115150
J:261678




Genotype
MGI:6159580
ht2
Allelic
Composition
Map2k1tm2.1Chrn/Map2k1+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map2k1tm2.1Chrn mutation (1 available); any Map2k1 mutation (92 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• pulmonary artery stenosis is observed at E13.5 left
• left and right pulmonary artery lumen areas are reduced




Genotype
MGI:6159582
ht3
Allelic
Composition
Map2k1tm2.1Chrn/Map2k1tm1.1Chrn
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map2k1tm1.1Chrn mutation (0 available); any Map2k1 mutation (92 available)
Map2k1tm2.1Chrn mutation (1 available); any Map2k1 mutation (92 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• pulmonary artery stenosis is observed at E13.5
• left and right pulmonary artery lumen areas are reduced

craniofacial

skeleton

vision/eye
• width of the inner canthal distance is increased





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
04/23/2024
MGI 6.23
The Jackson Laboratory