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Phenotypes Associated with This Genotype
Genotype
MGI:6159581
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 (94 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


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
11/05/2024
MGI 6.24
The Jackson Laboratory