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Symbol
Name
ID
Actg1
actin, gamma, cytoplasmic 1
MGI:87906
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Postnatal microcephaly
Lissencephaly
Pachygyria
Agenesis of corpus callosum
Ventriculomegaly
Intellectual disability
Global developmental delay
Seizures
Disease(s) Associated with ACTG1
Baraitser-Winter syndrome

Mouse Phenotypes
abnormal cochlear hair cell stereociliary bundle morphology
decreased outer hair cell stereocilia number
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
02/11/2020
MGI 6.14
The Jackson Laboratory