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Literature summary for 4.1.3.16 extracted from

  • Belostotsky, R.; Seboun, E.; Idelson, G.H.; Milliner, D.S.; Becker-Cohen, R.; Rinat, C.; Monico, C.G.; Feinstein, S.; Ben-Shalom, E.; Magen, D.; Weissman, I.; Charon, C.; Frishberg, Y.
    Mutations in DHDPSL are responsible for primary hyperoxaluria type III (2010), Am. J. Hum. Genet., 87, 392-399.
    View publication on PubMedView publication on EuropePMC
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Localization

Localization Comment Organism GeneOntology No. Textmining
mitochondrion
-
 Homo sapiens 5739
-

Organism

Organism UniProt Comment Textmining
Homo sapiens Q86XE5
-
-

Synonyms

Synonyms Comment Organism
4-hydroxy-2-oxoglutarate aldolase
-
 Homo sapiens
DHDPSL
-
 Homo sapiens
dihydrodipicolinate synthase-like enzyme
-
 Homo sapiens

General Information

General Information Comment Organism
malfunction mutations are responsible for primary hyperoxaluria type III Homo sapiens