|
Symbol Name ID |
Actg1
actin, gamma, cytoplasmic 1 MGI:87906 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal pinna morphology |
Bilateral sensorineural hearing impairment |
Progressive sensorineural hearing impairment |
Hearing impairment |
| Disease(s) Associated with ACTG1 | ||||
| autosomal dominant nonsyndromic deafness 20 | ||||
| Baraitser-Winter syndrome 2 |
| Mouse Phenotypes | abnormal cochlear hair cell stereociliary bundle morphology |
decreased outer hair cell stereocilia number |
increased or absent threshold for auditory brainstem response |
increased susceptibility to age-related hearing loss |
impaired hearing |
deafness |
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| Availability | Mouse Genotype | ||||||
| Actg1tm1.1Erv/Actg1tm1.1Erv | |||||||
| Actg1tm1Erv/Actg1tm1.1Erv | |||||||
| Actg1tm1.2Erv/Actg1tm1.2Erv 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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