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.
R64-1-1:BK006934.2
This gene has 1 transcript (splice variant), 457 orthologues, 8 paralogues and is a member of 1 Ensembl protein family.
Name | Transcript ID | bp | Protein | Translation ID | Biotype | UniProt | RefSeq | Flags |
---|---|---|---|---|---|---|---|---|
PUT2 | YHR037W_mRNA | 1728 | 575aa | YHR037W | Protein coding | P07275 | - | Ensembl Canonical, |