|
Symbol Name ID |
Actb
actin, beta MGI:87904 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Ventriculomegaly |
Lissencephaly |
Pachygyria |
Agenesis of corpus callosum |
Intellectual disability |
Global developmental delay |
Seizure |
| Disease(s) Associated with ACTB | ||||||||
| Baraitser-Winter syndrome 1 |
| Mouse Phenotypes | abnormal cochlear hair cell stereociliary bundle morphology |
abnormal outer hair cell stereociliary bundle morphology |
short outer hair cell stereocilia |
decreased outer hair cell stereocilia number |
short cochlear hair cell stereocilia |
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| Availability | Mouse Genotype | |||||
| Actbem1Erv/Actbem1Erv | ||||||
| Actbtm1.1Erv/Actbtm1.1Erv Tg(Atoh1-cre)1Bfri/? (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 04/23/2024 MGI 6.23 |
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