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Symbol
Name
ID

Aldh1a2
aldehyde dehydrogenase family 1, subfamily A2
MGI:107928

Phenotype annotations related to muscle

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Congenital diaphragmatic hernia	Aplasia/Hypoplasia of the diaphragm	Agenesis of the diaphragm
Disease(s) Associated with ALDH1A2
congenital diaphragmatic hernia

Mouse Phenotypes		muscle phenotype	abnormal myocardium layer morphology	absent myocardial trabeculae	thick myocardium
Availability	Mouse Genotype	muscle phenotype	abnormal myocardium layer morphology	absent myocardial trabeculae	thick myocardium
	Aldh1a2^tm1Ipc/Aldh1a2^tm1Ipc
	Aldh1a2^tm1Dll/Aldh1a2^tm1Ipc Tg(Rarb-cre)1Mrc/0 (conditional)	*

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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