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Symbol Name ID |
Kptn
kaptin MGI:1890380 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Dolichocephaly |
Scaphocephaly |
Mandibular prognathia |
Retrognathia |
Macrocephaly |
Prominent forehead |
High palate |
Broad nasal tip |
Downslanted palpebral fissures |
| Disease(s) Associated with KPTN | ||||||||||
| autosomal recessive intellectual developmental disorder 41 |
| Mouse Phenotypes | abnormal cranium morphology |
enlarged cranium |
increased cranium height |
increased cranium length |
increased cranium width |
frontal bossing |
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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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