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Symbol Name ID |
Kptn
kaptin MGI:1890380 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Autistic behavior |
Motor stereotypy |
Self-injurious behavior |
| Disease(s) Associated with KPTN | |||
| autosomal recessive intellectual developmental disorder 41 |
| Mouse Phenotypes | behavior/neurological phenotype |
abnormal behavior |
abnormal long-term spatial reference memory |
increased anxiety-related response |
abnormal response to social novelty |
increased locomotor activity |
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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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