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Protein Coding Gene : Hoga1 4-hydroxy-2-oxoglutarate aldolase 1

Primary Identifier  MGI:1914682 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  67432
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable 4-hydroxy-2-oxoglutarate aldolase activity; N-acetylneuraminate lyase activity; and protein homodimerization activity. Predicted to be involved in carboxylic acid metabolic process. Located in mitochondrion. Used to study primary hyperoxaluria. Human ortholog(s) of this gene implicated in primary hyperoxaluria type 3. Orthologous to human HOGA1 (4-hydroxy-2-oxoglutarate aldolase 1).
PHENOTYPE: Mice homozygous for a knock-out allele exhibit normal urinary excretion of oxalate but show increased urine 2,4-dihydroxyglutarate (DHG) levels especially when challenged by the inclusion of hydroxyproline in the diet. [provided by MGI curators]
  • synonyms:
  • N-acetylneuraminate pyruvate lyase 2 (putative),
  • 4-hydroxy-2-oxoglutarate aldolase 1,
  • dihydrodipicolinate synthase-like, mitochondrial,
  • RIKEN cDNA 0610010D20 gene,
  • 0610010D20Rik,
  • Hoga1,
  • Npl2,
  • Dhdpsl

Features --> Cross References

Genome

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

0 Involved In Mutations

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0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

3 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

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0 Driver For