|
Symbol Name ID |
Trappc9
trafficking protein particle complex 9 MGI:1923760 |
| Darker colors indicate more annotations |
| Human Phenotypes | Secondary microcephaly |
Abnormal cerebral white matter morphology |
Hypoplasia of the corpus callosum |
Inferior cerebellar vermis hypoplasia |
Delayed speech and language development |
Hyperactivity |
Bruxism |
Recurrent hand flapping |
Intellectual disability |
Global developmental delay |
Delayed ability to walk |
Seizure |
| Disease(s) Associated with TRAPPC9 | ||||||||||||
| autosomal recessive intellectual developmental disorder 13 |
| Mouse Phenotypes | absent segment of posterior cerebral artery |
multiple persisting craniopharyngeal ducts |
decreased brain weight |
decreased brain size |
abnormal lateral ventricle morphology |
abnormal corpus callosum morphology |
decreased corpus callosum size |
abnormal medulla oblongata morphology |
decreased substantia nigra size |
abnormal pons morphology |
increased striatum size |
small thalamus |
decreased cingulate cortex size |
decreased hippocampal fimbria size |
decreased hippocampus volume |
hippocampus atrophy |
abnormal cerebral cortex morphology |
decreased primary motor cortex size |
abnormal cerebellum morphology |
astrocytosis |
abnormal dopaminergic neuron morphology |
abnormal dorsal root ganglion morphology |
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| Availability | Mouse Genotype | ||||||||||||||||||||||
| Trappc9em1Xyli/Trappc9em1Xyli | |||||||||||||||||||||||
| Trappc9tm1a(EUCOMM)Wtsi/Trappc9tm1a(EUCOMM)Wtsi | |||||||||||||||||||||||
| Trappc9tm1a(EUCOMM)Wtsi/Trappc9+ | |||||||||||||||||||||||
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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