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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Acta1
actin alpha 1, skeletal muscle
MGI:87902
22 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Acta1tm1Hrd/Acta1+
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6JArc)
abnormal muscle fiber morphology J:184588
abnormal sarcomere morphology J:184588
blepharoptosis J:184588
decreased body weight J:184588
decreased grip strength J:184588
decreased locomotor activity J:184588
decreased muscle weight J:184588
excessive tearing J:184588
facial muscle atrophy J:184588
premature death J:184588
Acta1tm1Jll/Acta1tm1Jll
involves: 129P2/OlaHsd * Black Swiss
abnormal muscle development J:78070
abnormal muscle physiology J:78070
abnormal skeletal muscle fiber morphology J:78070
decreased body size J:78070
decreased body weight J:78070
decreased brown adipose tissue amount J:78070
decreased glycogen level J:78070
decreased liver glycogen level J:78070
decreased skeletal muscle fiber diameter J:78070
decreased skeletal muscle glycogen level J:78070
muscle weakness J:78070
postnatal lethality, complete penetrance J:78070
scoliosis J:78070

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
04/16/2024
MGI 6.23
The Jackson Laboratory