|
Symbol Name ID |
Actb
actin, beta MGI:87904 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Overfolded helix |
Low-set ears |
Sensorineural hearing impairment |
| Disease(s) Associated with ACTB | |||
| Baraitser-Winter syndrome 1 |
| Mouse Phenotypes | hearing/vestibular/ear phenotype |
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 |
increased or absent threshold for auditory brainstem response |
increased susceptibility to age-related hearing loss |
impaired hearing |
|
| Availability | Mouse Genotype | |||||||||
| Actbem1Erv/Actbem1Erv | ||||||||||
| Actbtm1.1Erv/Actbtm1.1Erv Foxg1tm1(cre)Skm/Foxg1+ (conditional) |
* | |||||||||
| Actbtm1.1Erv/Actbtm1.1Erv Tg(Atoh1-cre)1Bfri/? (conditional) |
* | |||||||||
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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