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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cmya5
cardiomyopathy associated 5
MGI:1923719
22 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Cmya5tm1Cap/Cmya5tm1Cap
129-Cmya5tm1Cap
abnormal cardiac muscle tissue morphology J:322761
abnormal cerebellum morphology J:322761
abnormal gastrocnemius morphology J:322761
abnormal intercalated disk morphology J:322761
abnormal nervous system dopamine level J:322761
abnormal Purkinje cell dendrite morphology J:322761
abnormal sarcoplasmic reticulum morphology J:322761
abnormal social recognition J:322761
abnormal soleus morphology J:322761
anhedonia J:322761
normal behavior/neurological phenotype J:322761
cardiac interstitial fibrosis J:322761
decreased startle reflex J:322761
decreased ventricle muscle contractility J:322761
dilated heart atrium J:322761
increased heart atrium size J:322761
increased prepulse inhibition J:322761
increased serotonin level J:322761
increased thigmotaxis J:322761
lipofuscinosis J:322761
perivascular fibrosis J:322761
thick ventricular wall J:322761

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
04/30/2024
MGI 6.23
The Jackson Laboratory