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Symbol
Name
ID
Actg1
actin, gamma, cytoplasmic 1
MGI:87906
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Muscular hypotonia
Generalized hypotonia
Disease(s) Associated with ACTG1
Baraitser-Winter syndrome

Mouse Phenotypes
abnormal Z line morphology
abnormal skeletal muscle fiber morphology
increased variability of skeletal muscle fiber size
centrally nucleated skeletal muscle fibers
impaired skeletal muscle contractility
Availability Mouse Genotype
Actg1tm1.2Erv/Actg1tm1.2Erv
Tg(ACTA1-cre)79Jme/0  (conditional)
Actg1tm1Erv/Actg1tm1Erv
Tg(ACTA1-cre)79Jme/0  (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
11/05/2019
MGI 6.14
The Jackson Laboratory