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Symbol
Name
ID
Eef1a2
eukaryotic translation elongation factor 1 alpha 2
MGI:1096317
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Hypotonia
Neonatal hypotonia
Generalized neonatal hypotonia
Disease(s) Associated with EEF1A2
autosomal dominant intellectual developmental disorder 38
developmental and epileptic encephalopathy 33

Mouse Phenotypes
abnormal muscle morphology
decreased skeletal muscle mass
Availability Mouse Genotype
Eef1a2wst/Eef1a2wst
Eef1a2em#Abb/Eef1a2+

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
04/09/2024
MGI 6.23
The Jackson Laboratory