GRHPR

OMIMHGNC

Synonym(s): PH2, GLXR

Locus: 9q12

Protein: GRHPR protein

 

Disorders

Tests

Test Type
Molecular (17)
Panel (3)
Test Method
Del/Dup (CNV) (4)
Sequencing, Capillary (Sanger) (10)
Genotyping (Microarray, Beads, etc.) (1)
Sequencing, Next Gen (5)
Prenatal/Carrier
Prenatal (2)
Carrier (6)
Lab Location
Germany(5)
USA(7)
Spain(2)
Portugal(2)
Poland(1)
 
TAT: 3-4 weeks
price: contact lab
GRHPR Sequencing
method(s): ◦ Sequencing, Capillary (Sanger) 
Center for Nephrology and Metabolic Disorders, Laboratory for Molecular Diagnostics - Weisswasser, Germany
TAT: 3-4 weeks
price: contact lab
GRHPR Del/Dup
method(s): ◦ Del/Dup (CNV) 
Center for Nephrology and Metabolic Disorders, Laboratory for Molecular Diagnostics - Weisswasser, Germany
GRHPR Gene, Full Gene Analysis
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Mayo Clinic - Minnesota, Molecular Genetics Laboratory - Rochester, MN, USA
GRHPR Gene, Known Mutation
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Mayo Clinic - Minnesota, Molecular Genetics Laboratory - Rochester, MN, USA
TAT: 3-4 weeks
price: $710.00
Primary Hyperoxaluria type 2 via the GRHPR Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA
Primary Hyperoxaluria
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) 
Cologne University, Institute of Human Genetics - Cologne, Germany
Primary Hyperoxaluria Type 2, Sequencing GRHPR Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
Reference Laboratory Genetics - Barcelona, Spain
TAT: 7-10 days
price: contact lab
Primary Hyperoxaluria: Type 2
method(s): ◦ Genotyping (Microarray, Beads, etc.) 
Recombine - Livingston, NJ, USA
Kidney Diseases Panel
method(s): ◦ Sequencing, Next Gen 
Genomic Laboratory of the DNA Research Center LTD (Centrum Badań DNA sp z o.o.) - Poznań, Poland
Hyperoxaluria primary type II (frequent mutations on GRHPR gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
Primary hyperoxaluria type 2 (sequence analysis of GRHPR gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
Primary Hyperoxaluria Type 2: GRHPR gene sequence analysis
method(s): ◦ Sequencing, Capillary (Sanger) 
GENETAQ, Molecular Genetics Centre - Malaga, Spain
TAT: 7-8 weeks
price: contact lab
Severe Recessive Childhood Diseases
method(s): ◦ Sequencing, Next Gen 
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany
Hyperoxaluria Panel
method(s): ◦ Sequencing, Next Gen 
CeGaT GmbH - Tübingen, Germany
TAT: 4-6 weeks
price: contact lab
Metabolic Disorders Gene Set
method(s): ◦ Sequencing, Next Gen 
Genomics and Pathology Services, Washington University - St. Louis, MO, USA
TAT: 4-5 Weeks
price: contact lab
GRHPR
method(s): ◦ Sequencing, Next Gen 
Fulgent Diagnostics - Temple City, CA, USA
TAT: 4-5 Weeks
price: contact lab
GRHPR
method(s): ◦ Sequencing, Capillary (Sanger) 
Fulgent Diagnostics - Temple City, CA, USA

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