Symbol Name ID |
Eef1a2
eukaryotic translation elongation factor 1 alpha 2 MGI:1096317 |
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 |
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Availability | Mouse Genotype | ||
Eef1a2wst/Eef1a2wst | |||
Eef1a2em#Abb/Eef1a2+ |
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 |
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