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Details of GRHPR gene in Homo sapiens
IDs |
Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
| GRHPR | GLXR | Q9UBQ7 | GRHPR_HUMAN | 9380 | Q9UKX1 | 2GCG 2H1S 2Q50 2WWR 2GCG 2H1S 2Q50 2WWR | progressive tissue |
Disease |
Disease |
OMIM id |
Hyperoxaluria primary 2 (HP2) [MIM:260000]: A disorder characterized by elevated urinary excretion of oxalate and L- glycerate |
nephrolithiasis |
Phenotypes
Abnormal urine anion concentration, Abnormality of amino acid metabolism, Abnormality of carboxylic acid metabolism, Abnormality of metabolism/homeostasis, Abnormality of the genitourinary system, Abnormality of the kidney, Abnormality of the upper urinary tract, Abnormality of the urinary system, Abnormality of the urinary system physiology, Abnormality of urine homeostasis, Aciduria, All, Aminoaciduria, Autosomal recessive inheritance, Calcium nephrolithiasis, Calcium oxalate nephrolithiasis, Hyperoxaluria, Mode of inheritance, Nephrolithiasis, Phenotypic abnormality.
Orthologs in other species |
M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
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