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Symbol Name ID |
Chuk
conserved helix-loop-helix ubiquitous kinase MGI:99484 |
| Darker colors indicate more annotations |
| Human Phenotypes | Omphalocele |
Congenital diaphragmatic hernia |
| Disease(s) Associated with CHUK | ||
| fetal encasement syndrome |
| Mouse Phenotypes | abnormal tooth morphology |
abnormal incisor morphology |
small incisors |
abnormal molar cusp morphology |
abnormal tooth color |
abnormal enamel knot morphology |
abnormal nasal capsule morphology |
palatal shelves fail to meet at midline |
cleft secondary palate |
cleft palate |
small nasal septum |
short snout |
shortened head |
anotia |
esophagus hyperplasia |
decreased birth body size |
weight loss |
omphalocele |
abnormal head morphology |
postnatal growth retardation |
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| Availability | Mouse Genotype | ||||||||||||||||||||
| Chuktm1.1Mpa/Chuktm1.1Mpa | |||||||||||||||||||||
| Chuktm1Aki/Chuktm1Aki | |||||||||||||||||||||
| Chuktm1Mka/Chuktm1Mka | |||||||||||||||||||||
| Chuktm1Ver/Chuktm1Ver | |||||||||||||||||||||
| Chuktm2Yhu/Chuktm2Yhu | |||||||||||||||||||||
| Chukem1(IMPC)Ccpcz/Chuk+ | |||||||||||||||||||||
| Chuktm1Mpa/Chuktm1Mpa Tg(KRT14-cre)1Cgn/? (conditional) |
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| Chuktm1Yhu/Chuktm1Yhu Tg(KRT5-cre)5132Jlj/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 04/09/2024 MGI 6.23 |
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