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HOGA1 4-hydroxy-2-oxoglutarate aldolase 1

Gene ID: 112817, updated on 5-Mar-2024
Gene type: protein coding
Also known as: HP3; NPL2; DHDPS2; DHDPSL; C10orf65

Summary

The authors of PMID:20797690 cloned this gene while searching for genes in a region of chromosome 10 linked to primary hyperoxalurea type III. They noted that even though the encoded protein has been described as a mitochondrial dihydrodipicolinate synthase-like enzyme, it shares little homology with E. coli dihydrodipicolinate synthase (Dhdps), particularly in the putative substrate-binding region. Moreover, neither lysine biosynthesis nor sialic acid metabolism, for which Dhdps is responsible, occurs in vertebrate mitochondria. They propose that this gene encodes mitochondrial 4-hydroxyl-2-oxoglutarate aldolase (EC 4.1.3.16), which catalyzes the final step in the metabolic pathway of hydroxyproline, releasing glyoxylate and pyruvate. This gene is predominantly expressed in the liver and kidney, and mutations in this gene are found in patients with primary hyperoxalurea type III. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Nov 2010]

Associated conditions

See all available tests in GTR for this gene

DescriptionTests
Genome-wide association study identifies multiple loci influencing human serum metabolite levels.
GeneReviews: Not available
Primary hyperoxaluria type 3See labs

Genomic context

Location:
10q24.2
Sequence:
Chromosome: 10; NC_000010.11 (97584389..97612802)
Total number of exons:
7

Links

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