|
Symbol Name ID |
Kptn
kaptin MGI:1890380 |
| Darker colors indicate more annotations |
| Human Phenotypes | Ventriculomegaly |
Delayed speech and language development |
Anxiety |
Autistic behavior |
Motor stereotypy |
Self-injurious behavior |
Intellectual disability |
Global developmental delay |
Motor delay |
Bilateral tonic-clonic seizure |
Generalized non-motor (absence) seizure |
Generalized-onset seizure |
| Disease(s) Associated with KPTN | ||||||||||||
| autosomal recessive intellectual developmental disorder 41 |
| Mouse Phenotypes | increased brain size |
small lateral ventricles |
increased corpus callosum size |
increased brain internal capsule size |
small hippocampus |
increased cerebral cortex cell number |
increased cerebral cortex total cell area |
increased primary motor cortex size |
thickened cerebral cortex |
abnormal nervous system physiology |
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| Availability | Mouse Genotype | ||||||||||
| Kptntm1a(EUCOMM)Wtsi/Kptntm1a(EUCOMM)Wtsi | |||||||||||
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 04/16/2024 MGI 6.23 |
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