Automated description from the Alliance of Genome Resources (Release 9.0.0)
Enables succinate-semialdehyde dehydrogenase (NAD+) activity. Acts upstream of or within oxoacid metabolic process and post-embryonic development. Located in mitochondrion. Is active in mitochondrial matrix. Used to study epilepsy. Human ortholog(s) of this gene implicated in succinic semialdehyde dehydrogenase deficiency. Orthologous to human ALDH5A1 (aldehyde dehydrogenase 5 family member A1).
This site uses cookies.
Some cookies are essential for site operations and others help us analyze use and utility of our web site.
Please refer to our
privacy policy
for more information.