|
Symbol Name ID |
Minpp1
multiple inositol polyphosphate histidine phosphatase 1 MGI:1336159 |
| Darker colors indicate more annotations |
| Human Phenotypes | Dysphagia |
Spastic tetraplegia |
Hypoplasia of the pons |
Ventriculomegaly |
Cerebral cortical atrophy |
Thin corpus callosum |
Cerebellar hypoplasia |
Abnormality of extrapyramidal motor function |
Absent speech |
Delayed fine motor development |
Delayed gross motor development |
Seizure |
| Disease(s) Associated with MINPP1 | ||||||||||||
| pontocerebellar hypoplasia type 16 |
| Mouse Phenotypes | decreased brain weight |
thin cerebral cortex |
abnormal neuron physiology |
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| Availability | Mouse Genotype | |||
| Minpp1em1Vca/Minpp1em1Vca | ||||
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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