|
Symbol Name ID |
Spr
sepiapterin reductase MGI:103078 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Oculomotor apraxia |
Spasticity |
Frequent falls |
Ataxia |
Bradykinesia |
Choreoathetosis |
Cerebral palsy |
Tremor |
Delayed speech and language development |
Dysarthria |
Depression |
Atypical behavior |
Aggressive behavior |
Hyperactivity |
Cognitive impairment |
Intellectual disability |
Drowsiness |
Sleep abnormality |
Hyperreflexia |
Dystonia |
Oculogyric crisis |
Global developmental delay |
Motor delay |
Seizure |
| Disease(s) Associated with SPR | |||||||||||||||||||||||||
| sepiapterin reductase deficiency |
| Mouse Phenotypes | abnormal dopaminergic neuron morphology |
abnormal synaptic neurotransmitter level |
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| Availability | Mouse Genotype | ||
| Sprtm1Spo/Sprtm1Spo | |||
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 05/07/2024 MGI 6.23 |
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