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Protein Coding Gene : Grhpr glyoxylate reductase/hydroxypyruvate reductase

Primary Identifier  MGI:1923488 Organism  mouse, laboratory
Chromosome  4 NCBI Gene Number  76238
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable several functions, including adenyl nucleotide binding activity; oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor; and protein homodimerization activity. Predicted to be involved in dicarboxylic acid metabolic process and glyoxylate metabolic process. Predicted to be located in cytoplasm. Predicted to be part of catalytic complex. Predicted to be active in cytosol. Is expressed in several structures, including adrenal gland; alimentary system; genitourinary system; integumental system; and nervous system. Used to study primary hyperoxaluria type 2. Human ortholog(s) of this gene implicated in primary hyperoxaluria and primary hyperoxaluria type 2. Orthologous to human GRHPR (glyoxylate and hydroxypyruvate reductase).
PHENOTYPE: Mice homozygous for a gene trap allele exhibit primary hyperoxaluria. [provided by MGI curators]
  • synonyms:
  • 6430629L09Rik,
  • Grhpr,
  • MGI:1916037,
  • glyoxylate reductase/hydroxypyruvate reductase,
  • RIKEN cDNA 6430629L09 gene,
  • RIKEN cDNA 1110059D05 gene,
  • 1110059D05Rik

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Genome

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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

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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