aldehyde dehydrogenase 6 family, member A1

Symbol

ALDH6A1 (may also be known as: None)

Organism

Human

Description

This gene encodes a member of the aldehyde dehydrogenase protein family. The encoded protein is a mitochondrial methylmalonate semialdehyde dehydrogenase that plays a role in the valine and pyrimidine catabolic pathways. This protein catalyzes the irreversible oxidative decarboxylation of malonate and methylmalonate semialdehydes to acetyl- and propionyl-CoA. Methylmalonate semialdehyde dehydrogenase deficiency is characterized by elevated beta-alanine, 3-hydroxypropionic acid, and both isomers of 3-amino and 3-hydroxyisobutyric acids in urine organic acids. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013]

Orthologs

SymbolSpecies
alh-8 Caenorhabditis elegans
CG17896 Drosophila melanogaster
aldh6a1 Danio rerio
Aldh6a1 Mus musculus
Aldh6a1 Rattus norvegicus

Links to external resources

Changes associated with this gene

GO Terms

GO IDGO TermGO Category
GO:0006573 valine metabolic process biological_process
GO:0009083 branched chain family amino acid catabolic process biological_process
GO:0019859 thymine metabolic process biological_process
GO:0034641 cellular nitrogen compound metabolic process biological_process
GO:0044281 small molecule metabolic process biological_process
GO:0005634 nucleus cellular_component
GO:0005730 nucleolus cellular_component
GO:0005739 mitochondrion cellular_component
GO:0005759 mitochondrial matrix cellular_component
GO:0000062 fatty-acyl-CoA binding molecular_function
GO:0004491 methylmalonate-semialdehyde dehydrogenase (acylating) activity molecular_function
GO:0016491 oxidoreductase activity molecular_function
GO:0018478 malonate-semialdehyde dehydrogenase (acetylating) activity molecular_function