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 |
|
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 12/17/2024 MGI 6.24 |
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