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Symbol
Name
ID
Actg1
actin, gamma, cytoplasmic 1
MGI:87906
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Sensorineural hearing impairment
Bilateral sensorineural hearing impairment
Progressive sensorineural hearing impairment
Low-set ears
Abnormality of the pinna
Overfolded helix
Hearing impairment
Disease(s) Associated with ACTG1
autosomal dominant nonsyndromic deafness 20
Baraitser-Winter syndrome

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
Availability Mouse Genotype
Actg1tm1.1Erv/Actg1tm1.1Erv
Actg1tm1Erv/Actg1tm1.1Erv
Actg1tm1.2Erv/Actg1tm1.2Erv
Tg(Atoh1-cre)1Bfri/?  (conditional)

Contributing Projects:
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
11/12/2019
MGI 6.14
The Jackson Laboratory