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Phenotypes Associated with This Genotype
Genotype
MGI:5573137
Allelic
Composition
McuGt(IST11669F8)Tigm/McuGt(IST11669F8)Tigm
Genetic
Background
involves: C57BL/6 * C57BL/6N * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
McuGt(IST11669F8)Tigm mutation (0 available); any Mcu mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
N
• mice exhibit normal total body oxygen consumption
• increased serum lactate levels

cellular
N
• mice exhibit normal cell death
• mitochondria from skeletal muscle, mouse embryonic fibroblast and adult cardiac myocytes exhibit impaired calcium uptake compared with wild-type mitochondria
• cardiac and hepatic mitochondria fail to exhibit calcium-induced permeability transition pore opening unlike in wild-type mitochondria

growth/size/body

behavior/neurological

cardiovascular system
N
• mice exhibit normal response to ischemia-reperfusion injury


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
01/28/2026
MGI 6.24
The Jackson Laboratory