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Symbol
Name
ID
Aldh1a2
aldehyde dehydrogenase family 1, subfamily A2
MGI:107928
Phenotype annotations related to cardiovascular system
Darker colors indicate more annotations
Human Phenotypes
Abnormal cardiovascular system morphology
Disease(s) Associated with ALDH1A2
congenital diaphragmatic hernia

Mouse Phenotypes
abnormal artery morphology
abnormal pharyngeal arch artery morphology
abnormal third pharyngeal arch artery morphology
absent pharyngeal arch arteries
abnormal aortic arch and aortic arch branch attachment
aberrant origin of the right subclavian artery
cervical aortic arch
right aortic arch
double aortic arch
abnormal common carotid artery morphology
abnormal left subclavian artery morphology
abnormal vascular development
abnormal vitelline vasculature morphology
abnormal myocardium layer morphology
absent myocardial trabeculae
thick myocardium
conotruncal ridge hypoplasia
abnormal truncus arteriosus septation
persistent truncus arteriosus
abnormal heart development
abnormal fetal atrioventricular canal morphology
absent atrioventricular cushions
abnormal fetal cardiomyocyte morphology
failure of heart looping
abnormal heart tube morphology
ventricular septal defect
enlarged heart
Availability Mouse Genotype
Aldh1a2grim/Aldh1a2grim
Aldh1a2tm1Dll/Aldh1a2tm1Dll
Aldh1a2tm1Gdu/Aldh1a2tm1Gdu
Aldh1a2tm1Ipc/Aldh1a2tm1Ipc
Aldh1a2tm1Dll/Aldh1a2tm1Ipc

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
04/23/2024
MGI 6.23
The Jackson Laboratory