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Newborns main panel

Gene: GRHPR

Green List (high evidence)
GRHPR (glyoxylate and hydroxypyruvate reductase)
EnsemblGeneIds (GRCh38): ENSG00000137106
EnsemblGeneIds (GRCh37): ENSG00000137106
OMIM: 604296, Gene2Phenotype
GRHPR is in 6 panels

1 review

Mafalda Gomes (Genomics England Curator)

The mechanism of pathogenicity is loss-of-function (LOF).
Created: 1 Jun 2023, 2:40 p.m. | Last Modified: 1 Jun 2023, 2:40 p.m.
Panel Version: 0.137
Ethnic differences in GRHPR mutations in patients with primary hyperoxaluria type 2 - PubMed (nih.gov)
Created: 1 Jun 2023, 12:22 p.m. | Last Modified: 1 Jun 2023, 12:22 p.m.
Panel Version: 0.134
Created: 1 Jun 2023, 12:22 p.m.
Last Modified: 1 Jun 2023, 12:22 p.m.
Panel version: 0.137

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
Phenotypes
  • Hyperoxaluria, primary, type II
OMIM
604296
Clinvar variants
Variants in GRHPR
Penetrance
None
Panels with this gene

History Filter Activity

14 Sep 2023, Gel status: 3

Set Phenotypes

Mafalda Gomes (Genomics England Curator)

Added phenotypes Hyperoxaluria, primary, type II for gene: GRHPR

5 Jul 2023, Gel status: 3

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Green was added to GRHPR. Added phenotypes Hyperoxaluria, primary, type II for gene: GRHPR Rating Changed from Amber List (moderate evidence) to Green List (high evidence)

31 May 2023, Gel status: 2

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Amber was added to GRHPR. Added phenotypes Hyperoxaluria, primary, type II for gene: GRHPR Rating Changed from No List (delete) to Amber List (moderate evidence)

5 May 2023, Gel status: 0

Added New Source, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Removed was added to GRHPR. Rating Changed from Amber List (moderate evidence) to No List (delete)

9 Mar 2023, Gel status: 2

Set Phenotypes

Mafalda Gomes (Genomics England Curator)

Added phenotypes Hyperoxaluria, primary, type II for gene: GRHPR

9 Mar 2023, Gel status: 2

Created, Added New Source, Set mode of inheritance

Mafalda Gomes (Genomics England Curator)

gene: GRHPR was added gene: GRHPR was added to Newborns main panel. Sources: Expert Review Amber Mode of inheritance for gene: GRHPR was set to BIALLELIC, autosomal or pseudoautosomal