Symbol Name ID |
Eif2b5
eukaryotic translation initiation factor 2B, subunit 5 epsilon MGI:2446176 |
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 |
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Availability | Mouse Genotype | |||||
Eif2b5tm1.1Sidr/Eif2b5tm1.1Sidr | ||||||
Eif2b5tm1.1Vdk/Eif2b5tm1.1Vdk | ||||||
Eif2b5tm1Itl/Eif2b5tm1Itl |
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 |
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