About Help FAQ

Symbol
Name
ID

Aifm1
apoptosis-inducing factor, mitochondrion-associated 1
MGI:1349419

Phenotype annotations related to behavior/neurological

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Feeding difficulties in infancy
Disease(s) Associated with AIFM1	Feeding difficulties in infancy
combined oxidative phosphorylation deficiency 6

Mouse Phenotypes		behavior/neurological phenotype	lethargy	abnormal seizure response to pharmacological agent	abnormal motor capabilities/coordination/movement	tremors	ataxia	impaired coordination	abnormal gait
Availability	Mouse Genotype	behavior/neurological phenotype	lethargy	abnormal seizure response to pharmacological agent	abnormal motor capabilities/coordination/movement	tremors	ataxia	impaired coordination	abnormal gait
	Aifm1^Hq/Aifm1^Hq
	Aifm1^Hq/Aifm1⁺	*
	Aifm1^Hq/Y
	Aifm1^tm2Pngr/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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/30/2024 MGI 6.23