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Symbol Name ID |
Ext1
exostosin glycosyltransferase 1 MGI:894663 |
| Darker colors indicate more annotations |
| Human Phenotypes | Dysphagia |
Peripheral nerve compression |
Cervical myelopathy |
Tethered cord |
Spinal cord compression |
Syringomyelia |
Somatic sensory dysfunction |
| Disease(s) Associated with EXT1 | |||||||
| hereditary multiple exostoses |
| Mouse Phenotypes | abnormal axon guidance |
abnormal brain development |
abnormal brain commissure morphology |
absent corpus callosum |
absent hippocampal commissure |
absent anterior commissure |
absent inferior colliculus |
abnormal cerebral cortex morphology |
thin cerebral cortex |
absent olfactory bulb |
absent cerebellum |
abnormal synaptic transmission |
abnormal excitatory postsynaptic currents |
reduced AMPA-mediated synaptic currents |
abnormal miniature excitatory postsynaptic currents |
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| Availability | Mouse Genotype | |||||||||||||||
| Ext1tm1Yama/Ext1tm1Yama Tg(Nes-cre)1Kln/0 (conditional) |
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| Ext1tm1Yama/Ext1tm1Yama Tg(Camk2a-cre)2834Lusc/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 04/23/2024 MGI 6.23 |
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