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Symbol Name ID |
Ufm1
ubiquitin-fold modifier 1 MGI:1915140 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Spasticity |
Cerebral atrophy |
Cerebellar atrophy |
Absent speech |
Intellectual disability |
Dystonia |
Seizure |
| Disease(s) Associated with UFM1 | ||||||||
| hypomyelinating leukodystrophy 14 |
| Mouse Phenotypes | increased neuron apoptosis |
increased brain apoptosis |
abnormal brain development |
decreased midbrain size |
small thalamus |
decreased neocortex size |
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| Availability | Mouse Genotype | ||||||
| Ufm1tm1.1Kmts/Ufm1tm1.1Kmts Tg(Nes-cre)1Kln/0 (conditional) |
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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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