- reductase/hydroxypyruvate
reductase is an
enzyme that in
humans is
encoded by the
GRHPR gene. This gene
encodes an
enzyme with
hydroxypyruvate reductase, glyoxylate...
-
deficient despite being catalytically active. Type II is ****ociated with
GRHPR.
Secondary hyperoxaluria can
occur as a
complication of
jejunoileal byp****...
-
provide a
flexible tool for
metabolic studies in plants. A
human protein,
GRHPR, has been
identified that
exhibits both
glyoxylate and
hydroxypyruvate reductase...
- reductase/Hydroxypyruvate
reductase (
GRHPR) is the
glycerate dehydrogenase found,
predominantly in the liver, of
humans encoded by the gene
GRHPR.
Under physiological...
-
results in an
overproduction of oxalate.
Mutations in the
genes AGXT and
GRHPR cause PH1 and PH2, respectively,
through decreased production or activity...
- 1:18,000,000
Hyperlysinemia A****
recessive Hyperoxaluria,
primary AGXT,
GRHPR,
DHDPSL Hyperphenylalaninemia 12q
Hypoalphalipoproteinemia (Tangier disease)...
-
primary hyperoxaluria type II),
which is ****ociated with
mutations in the
GRHPR (encoding for the
enzyme 'glyoxylate reductase/hydroxypyruvate reductase')...
-
transferase 1 GLE1L:
Nucleoporin GLE1 GPR107: G protein-coupled
receptor 107
GRHPR:
glyoxylate redasductase/hydroxypyruvate
reductase GSN:
cytoplasmic and...
- HGNC:17923 Q9NZI5 6623 GRHL2 HGNC:2799 Q6ISB3 6624 GRHL3 HGNC:25839 Q8TE85 6625
GRHPR HGNC:4570 Q9UBQ7 6626 GRIA1 HGNC:4571 P42261 6627 GRIA2 HGNC:4572 P42262...
- primary, type 1; 259900; AGXT Hyperoxaluria, primary, type II; 260000;
GRHPR Hyperoxaluria, primary, type III; 613616;
DHDPSL Hyperparathyroidism, AD;...
