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Symbol
Name
ID
Aldh7a1
aldehyde dehydrogenase family 7, member A1
MGI:108186
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Hypoglycemia
Lactic acidosis
Disease(s) Associated with ALDH7A1
pyridoxine-dependent epilepsy

Mouse Phenotypes
abnormal amino acid level
decreased glycine level
increased leucine level
decreased lysine level
increased ornithine level
increased phenylalanine level
increased proline level
increased serine level
increased circulating noradrenaline level
abnormal vitamin level
abnormal amino acid metabolism
Availability Mouse Genotype
Aldh7a1tm1d(EUCOMM)Hmgu/Aldh7a1tm1d(EUCOMM)Hmgu

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