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Symbol Name ID |
Kat6b
K(lysine) acetyltransferase 6B MGI:1858746 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Intellectual disability |
Global developmental delay |
Specific learning disability |
Seizure |
| Disease(s) Associated with KAT6B | |||||
| Ohdo syndrome, SBBYS variant |
| Mouse Phenotypes | abnormal neuronal migration |
abnormal telencephalon development |
abnormal cortical plate morphology |
decreased brain size |
decreased inferior colliculus size |
abnormal cerebral cortex morphology |
decreased cerebral cortex pyramidal cell number |
small olfactory bulb |
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| Availability | Mouse Genotype | ||||||||
| Kat6bGt(pKC199)1Pgr/Kat6bGt(pKC199)1Pgr | |||||||||
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 06/04/2024 MGI 6.13 |
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