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Symbol Name ID |
Pitrm1
pitrilysin metallepetidase 1 MGI:1916867 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cerebral atrophy |
Cerebellar atrophy |
Ataxia |
Dysmetria |
Tremor |
Titubation |
Psychotic episodes |
Compulsive behaviors |
Intellectual disability |
Intellectual disability, mild |
Brisk reflexes |
Unsteady gait |
Global developmental delay |
| Disease(s) Associated with PITRM1 | |||||||||||||
| autosomal recessive spinocerebellar ataxia 30 |
| Mouse Phenotypes | amyloid beta deposits |
gliosis |
neuron degeneration |
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| Availability | Mouse Genotype | |||
| Pitrm1tm1a(KOMP)Wtsi/Pitrm1+ | ||||
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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