|
Symbol Name ID |
Ube2a
ubiquitin-conjugating enzyme E2A MGI:102959 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypoplasia of the pons |
Abnormal cerebral white matter morphology |
Hypointensity of cerebral white matter on MRI |
Echolalia |
Absent speech |
Delayed speech and language development |
Poor speech |
Aggressive behavior |
Compulsive behaviors |
Self-injurious behavior |
Intellectual disability |
Intellectual disability, moderate |
Intellectual disability, severe |
Delayed gross motor development |
Seizure |
| Disease(s) Associated with UBE2A | |||||||||||||||
| syndromic X-linked intellectual disability Nascimento type |
| Mouse Phenotypes | reduced long-term depression |
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| Availability | Mouse Genotype | |
| Ube2atm1Agr/Y | ||
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 04/23/2024 MGI 6.23 |
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