|
Symbol Name ID |
Cdk13
cyclin dependent kinase 13 MGI:1916812 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Small cerebral cortex |
Agenesis of corpus callosum |
Hypoplasia of the corpus callosum |
Periventricular leukomalacia |
Spina bifida occulta |
Delayed speech and language development |
Autism |
Pica |
Intellectual disability |
Central sleep apnea |
Global developmental delay |
Motor delay |
Delayed ability to sit |
Delayed ability to walk |
Seizure |
Generalized non-motor (absence) seizure |
| Disease(s) Associated with CDK13 | |||||||||||||||||
| congenital heart defects, dysmorphic facial features, and intellectual developmental disorder |
| Mouse Phenotypes | delayed brain development |
decreased brain size |
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| Availability | Mouse Genotype | ||
| Cdk13tm1a(EUCOMM)Hmgu/Cdk13tm1a(EUCOMM)Hmgu | |||
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 04/30/2024 MGI 6.23 |
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