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 |
|
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) |
|||||||||||||||||||||
Chuktm1Yhu/Chuktm1Yhu Tg(KRT5-cre)5132Jlj/0 (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 09/03/2024 MGI 6.24 |
|
|