SLC22A12

OMIMHGNC

Synonym(s): OAT4L, RST, URAT1

Locus: 11q13.1

Protein: URAT1 transporter protein

 

Disorders

Tests

Test Type
Molecular (9)
Multi-Gene Panel (1)
Multi-Method Panel (2)
Test Method
Del/Dup (CNV) (1)
Sequencing, Capillary (Sanger) (8)
Sequencing, Next Gen (2)
Prenatal/Carrier
Prenatal (1)
Carrier (3)
Lab Location
Germany(2)
Portugal(1)
Spain(1)
USA(3)
Czech Republic(1)
Korea, Republic of(1)
 
Urate transporter SLC2A9 DysfunctionTest
method(s): ◦ Sequencing, Capillary (Sanger) 
General University Hospital in Prague, Institute of Inherited Metabolic Disorders - Praha, Czech Republic
URAT1-related hypouricemia test
method(s): ◦ Sequencing, Capillary (Sanger) 
Medical Genetics Center, Asan Medical Center - Seoul, Korea, Republic of
TAT: 3-4 weeks
price: contact lab
SLC22A12 Sequencing
method(s): ◦ Sequencing, Capillary (Sanger) 
Center for Nephrology and Metabolic Disorders, Laboratory for Molecular Diagnostics - Weisswasser, Germany
Hypouricemia renal (RHUC1, sequence analysis of SLC22A12 gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
Renal Hypouricemia Type 1, Sequencing SLC22A12 Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: 1-2 weeks
price: contact lab
Renal Hypouricemia Type 1
method(s): ◦ Sequencing, Capillary (Sanger) 
Alfred I. duPont Hospital for Children, Molecular Diagnostics Lab - Wilmington, DE, USA
TAT: 4-5 Weeks
price: contact lab
SLC22A12
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
TAT: 3-5 weeks
price: $1,940.00
Nephrolithiasis and Nephrocalcinosis Sequencing Panel
method(s): ◦ Sequencing, Next Gen 
PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA
TAT: 3-4 weeks
price: contact lab
Hypouricemia, renal type 1
method(s): ◦ Sequencing, Capillary (Sanger) 
Centogene AG, Rare Disease Company - Rostock, Germany