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Phenotypes Associated with This Genotype
Genotype
MGI:3779089
Allelic
Composition
Meox2tm1(cre)Sor/Meox2+
Mfn1tm2Dcc/Mfn1+
Mfn2tm1Dcc/Mfn2tm3Dcc
Genetic
Background
involves: 129S/SvEv * 129S4/SvJaeSor * Black Swiss
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Meox2tm1(cre)Sor mutation (3 available); any Meox2 mutation (18 available)
Mfn1tm2Dcc mutation (2 available); any Mfn1 mutation (44 available)
Mfn2tm1Dcc mutation (0 available); any Mfn2 mutation (26 available)
Mfn2tm3Dcc mutation (2 available); any Mfn2 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• after birth, about one third of mutant mice die on postnatal day 1
• mutant pups are born at appropriate Mendelian ratio
• mutant mice that survive the neonatal period die by P17

behavior/neurological
• mice surviving beyond P1 cannot easily regain posture when placed on their backs
• mice surviving beyond P1 display uncoordinated limb movements, and move primarily by writhing on their abdomen

growth/size/body
• mice surviving beyond P1 are severely runted, likely due to feeding problems secondary to their movement disorder


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
04/16/2024
MGI 6.23
The Jackson Laboratory