Acad9 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Acad9
acyl-Coenzyme A dehydrogenase family, member 9
MGI:1914272

13 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Acad9^{tm1a(KOMP)Wtsi}/Acad9^{tm1a(KOMP)Wtsi} involves: C57BL/6N	prenatal lethality, complete penetrance	J:326969
Acad9^{tm1c(KOMP)Wtsi}/Acad9^{tm1c(KOMP)Wtsi} Tg(ACTA1-cre)79Jme/0 involves: C57BL/6J * C57BL/6N * FVB/N * SJL	abnormal muscle morphology	J:326969
	centrally nucleated skeletal muscle fibers	J:326969
	impaired exercise endurance	J:326969
	lactic acidosis	J:326969
	muscle weakness	J:326969
Acad9^{tm1c(KOMP)Wtsi}/Acad9^{tm1c(KOMP)Wtsi} Tg(Myh6-cre)2182Mds/0 involves: C57BL/6N * FVB/N	abnormal heart morphology	J:326969
	abnormal mitochondrial physiology	J:326969
	cardiomyopathy	J:326969
	decreased cardiac muscle contractility	J:326969
	myocardial fiber disarray	J:326969
	postnatal lethality	J:326969
	thick ventricular wall	J:326969

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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