Symbol Name ID |
Cilk1
ciliogenesis associated kinase 1 MGI:1934157 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hydrocephalus |
Ventriculomegaly |
Focal polymicrogyria |
Agenesis of corpus callosum |
Absent septum pellucidum |
Aplasia of the olfactory bulb |
Aplasia/Hypoplasia of the cerebellum |
Holoprosencephaly |
Bilateral tonic-clonic seizure |
Generalized non-motor (absence) seizure |
Generalized myoclonic seizure |
Febrile seizure (within the age range of 3 months to 6 years) |
Disease(s) Associated with CILK1 | ||||||||||||
endocrine-cerebro-osteodysplasia syndrome | ||||||||||||
juvenile myoclonic epilepsy 10 |
Mouse Phenotypes | nervous system phenotype |
abnormal cervical flexure morphology |
hydrocephaly |
dilated brain ventricle |
|
Availability | Mouse Genotype | ||||
Cilk1tm1.1Zfu/Cilk1tm1.1Zfu | |||||
Cilk1tm1a(KOMP)Mbp/Cilk1tm1a(KOMP)Mbp | * |
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 07/05/2024 MGI 6.24 |
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