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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	Secondary microcephaly	Ventriculomegaly	Lissencephaly	Pachygyria	Agenesis of corpus callosum	Intellectual disability	Seizure
Disease(s) Associated with ACTG1
Baraitser-Winter syndrome 2

Mouse Phenotypes		spina bifida	abnormal cochlear hair cell stereociliary bundle morphology	decreased outer hair cell stereocilia number
Availability	Mouse Genotype	spina bifida	abnormal cochlear hair cell stereociliary bundle morphology	decreased outer hair cell stereocilia number
	Actg1^{tm1.1(KOMP)Vlcg}/Actg1^{tm1.1(KOMP)Vlcg}
	Actg1^tm1.1Erv/Actg1^tm1.1Erv
	Actg1^{tm1.1(KOMP)Vlcg}/Actg1⁺
	Actg1^tm1Erv/Actg1^tm1.1Erv
	Actg1^tm1.2Erv/Actg1^tm1.2Erv 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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