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Symbol
Name
ID

Acta1
actin alpha 1, skeletal muscle
MGI:87902

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement	Feeding difficulties	Feeding difficulties in infancy	Gastrostomy tube feeding in infancy	Tube feeding	Nasogastric tube feeding
Disease(s) Associated with ACTA1	Decreased fetal movement	Feeding difficulties	Feeding difficulties in infancy	Gastrostomy tube feeding in infancy	Tube feeding	Nasogastric tube feeding
congenital myopathy 2B
congenital myopathy 2C
nemaline myopathy 3

Mouse Phenotypes		decreased grip strength	decreased locomotor activity
Availability	Mouse Genotype
	Acta1^tm1Hrd/Acta1⁺

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23