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Symbol
Name
ID

Eif2b5
eukaryotic translation initiation factor 2B, subunit 5 epsilon
MGI:2446176

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement	Feeding difficulties	Atypical behavior	Apathy
Disease(s) Associated with EIF2B5
leukoencephalopathy with vanishing white matter

Mouse Phenotypes		ataxia	impaired coordination	decreased grip strength	abnormal locomotor activation	sporadic seizures
Availability	Mouse Genotype	ataxia	impaired coordination	decreased grip strength	abnormal locomotor activation	sporadic seizures
	Eif2b5^tm1.1Sidr/Eif2b5^tm1.1Sidr
	Eif2b5^tm1.1Vdk/Eif2b5^tm1.1Vdk
	Eif2b5^tm1Itl/Eif2b5^tm1Itl

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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