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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Aldh3a2
aldehyde dehydrogenase family 3, subfamily A2
MGI:1353452
17 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Aldh3a2tm1a(EUCOMM)Wtsi/Aldh3a2tm1a(EUCOMM)Wtsi
C57BL/6N-Aldh3a2tm1a(EUCOMM)Wtsi/Ics
abnormal behavior J:165965
decreased erythrocyte cell number J:165965
decreased hemoglobin content J:165965
decreased mean corpuscular volume J:165965
decreased prepulse inhibition J:165965
increased mean corpuscular volume J:165965
Aldh3a2tm1b(EUCOMM)Wtsi/Aldh3a2tm1b(EUCOMM)Wtsi
involves: C57BL * C57BL/6J * C57BL/6N * DBA
abnormal epidermis stratum basale morphology J:234695
abnormal epidermis stratum granulosum morphology J:234695
abnormal epidermis stratum spinosum morphology J:234695
abnormal keratinocyte physiology J:234695
abnormal lipid metabolism J:234695
abnormal phospholipid level J:234695
decreased aldehyde dehydrogenase activity J:234695
delayed skin barrier formation J:234695
increased food intake J:234695
increased keratinocyte proliferation J:234695
oxidative stress J:234695

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
04/16/2024
MGI 6.23
The Jackson Laboratory