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Symbol
Name
ID
Acta1
actin alpha 1, skeletal muscle
MGI:87902
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Mildly elevated creatine kinase
Chylothorax
Disease(s) Associated with ACTA1
congenital myopathy 2B
congenital myopathy 2C
nemaline myopathy 3

Mouse Phenotypes
decreased liver glycogen level
decreased skeletal muscle glycogen level
decreased glycogen level
Availability Mouse Genotype
Acta1tm1Jll/Acta1tm1Jll

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
05/14/2024
MGI 6.23
The Jackson Laboratory