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Symbol
Name
ID
Aifm1
apoptosis-inducing factor, mitochondrion-associated 1
MGI:1349419
Phenotype annotations related to cellular
Darker colors indicate more annotations
Human Phenotypes
Decreased activity of mitochondrial complex IV
Disease(s) Associated with AIFM1
combined oxidative phosphorylation deficiency 6

Mouse Phenotypes
increased cardiomyocyte apoptosis
abnormal mitochondrial morphology
abnormal mitochondrial crista morphology
increased mitochondrial number
abnormal cell physiology
abnormal cell cycle
increased cellular sensitivity to hydrogen peroxide
increased embryonic tissue cell apoptosis
decreased neuron apoptosis
decreased susceptibility to neuronal excitotoxicity
increased neuron apoptosis
abnormal aerobic respiration
abnormal respiratory electron transport chain
abnormal mitochondrial ATP synthesis coupled electron transport
abnormal mitochondrial physiology
decreased mitochondrial fission
oxidative stress
Availability Mouse Genotype
Aifm1Hq/Aifm1Hq
Aifm1tm2.1Pngr/Aifm1tm2.1Pngr
Aifm1Hq/Y
Aifm1tm1Pngr/Y
Aifm1tm2.1Pngr/Y
Aifm1tm2Pngr/Y
Foxg1tm1(cre)Skm/Foxg1+  (conditional)
Aifm1tm2Pngr/Y
Tg(Ckmm-cre)5Khn/0  (conditional)

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
04/30/2024
MGI 6.23
The Jackson Laboratory