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Phenotypes Associated with This Genotype
Genotype
MGI:3510873
Allelic
Composition
Mettm2Kln/Mettm2Kln
Genetic
Background
involves: 129/Sv * C57BL/6 * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mettm2Kln mutation (0 available); any Met mutation (82 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• born alive but died immediately after birth of respiratory failure

embryo
N
• placental development occurred when CD1 made up part of the genetic background

growth/size/body
• mildly reduced body weight

liver/biliary system
• liver structure loose with dissociated parenchymal cells
• liver weight reduced about 60%

muscle
• myoblasts fail to migrate into limbs
• 55% reduction in fetal myoblasts
• severely reduced diapragm
• severely reduced muscle mass in limbs, transverse sections of muscles reduced about 40%
• diaphragm muscle severely reduced

respiratory system
• occurs immediately after birth

nervous system
• motor axon outgrowth generally abnormal
• branches of the nervus thoracodorsalis were completely absent

cardiovascular system

cellular
• myoblasts fail to migrate into limbs


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
06/12/2024
MGI 6.13
The Jackson Laboratory