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Symbol
Name
ID

Aldh1a2
aldehyde dehydrogenase family 1, subfamily A2
MGI:107928

Phenotype annotations related to skeleton

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

Human Phenotypes	Prominent sternum
Disease(s) Associated with ALDH1A2	Prominent sternum
congenital diaphragmatic hernia

Mouse Phenotypes		skeleton phenotype	abnormal laryngeal cartilage morphology	abnormal cricoid cartilage morphology	abnormal thyroid cartilage morphology	abnormal tracheal cartilage morphology	decreased tracheal cartilage ring number
Availability	Mouse Genotype	skeleton phenotype	abnormal laryngeal cartilage morphology	abnormal cricoid cartilage morphology	abnormal thyroid cartilage morphology	abnormal tracheal cartilage morphology	decreased tracheal cartilage ring number
	Aldh1a2^tm1Dll/Aldh1a2^tm1Dll
	Aldh1a2^tm1Dll/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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