Delta-1-pyrroline-5-carboxylate dehydrogenase; nuclear-encoded mitochondrial protein involved in utilization of proline as sole nitrogen source; deficiency of human homolog ALDH4A1 causes type II hyperprolinemia (HPII), an autosomal recessive inborn error of metabolism; human homolog ALDH4A1 can complement yeast null mutant [Source:SGD;Acc:S000001079]

Chromosome VIII: 181,977-183,704 forward strand.

This transcript has 1 exon, is annotated with 10 domains and features, is associated with 38 variant alleles and maps to 29 oligo probes.

This transcript is a product of gene YHR037W Show transcript tableHide transcript table