UGT1A1

OMIMHGNC

Synonym(s): UGT1A, UGT1, GNT1

Locus: 2q37.1

Protein: Bilirubin UDP-glucronosyltrasferase 1-1

 

Disorders

Tests

Test Type
Molecular (58)
Multi-Gene Panel (14)
Multi-Method Panel (11)
Test Method
Microarray (CGH-Oligo, SNP, BAC) (1)
Del/Dup (CNV) (13)
Mutation Scanning of Entire Coding Region (1)
Sequencing, Capillary (Sanger) (27)
Genotyping (Microarray, Beads, etc.) (12)
Repeat Expansion / Contraction (3)
Sequencing, Next Gen (13)
Prenatal/Carrier
Prenatal (15)
Carrier (26)
Lab Location
USA(28)
Bulgaria(2)
Portugal(6)
Germany(9)
Turkey(2)
Spain(5)
Czech Republic(2)
Canada(2)
Finland(1)
Austria(1)
 
TAT: 1 week
price: contact lab
Gilbert Syndrome Test
method(s): ◦ Repeat Expansion / Contraction 
Detroit Medical Center University Laboratories, Molecular Genetics Diagnostic Laboratory - Detroit, MI, USA
UGT1A1 related disorders Test
method(s): ◦ Sequencing, Capillary (Sanger) 
bio.logis Center for Human Genetics - Frankfurt am Main, Germany
TAT: 4 weeks
price: contact lab
iGene Pharmacogenetics
method(s): ◦ Sequencing, Next Gen 
ApolloGen, Inc. - Irvine, CA, USA
TAT: 5-7 weeks
price: contact lab
iGene Comprehensive Panel (Cancer, Cardiac, Drug Sensitivity)
method(s): ◦ Sequencing, Next Gen 
ApolloGen, Inc. - Irvine, CA, USA
TAT: 3-4 weeks
price: contact lab
Gilbert Syndrome - UGT1A1 Gene -(TA) Repeat Number
method(s): ◦ Repeat Expansion / Contraction 
Biyolojik Bilimler Arastirma Gelistirme ve Uretim AS, Duzen Laboratuvarlar Grubu - Istanbul, Turkey
TAT: 1 week
price: contact lab
Irinotecan Toxicity (UGT1A1)
method(s): ◦ Sequencing, Capillary (Sanger) 
Biyolojik Bilimler Arastirma Gelistirme ve Uretim AS, Duzen Laboratuvarlar Grubu - Istanbul, Turkey
TAT: 2-3 weeks
price: contact lab
Gilbert Syndrome (UGT1A1 sequence analysis for promoter region)
method(s): ◦ Sequencing, Capillary (Sanger) 
Children's Hospital of Philadelphia, Division of Genomic Diagnostics - Philadelphia, PA, USA
Crigler-Najjar Syndrome
method(s): ◦ Sequencing, Capillary (Sanger) 
MVZ Dortmund Dr. Eberhard and Partner - Dortmund, Germany
Gilbert Syndrome
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Genotyping (Microarray, Beads, etc.) ◦ Del/Dup (CNV) 
MVZ Dortmund Dr. Eberhard and Partner - Dortmund, Germany
TAT: 3-4 weeks
price: contact lab
Neonatal and Adult Cholestasis: Sequencing Panel
method(s):
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA
TAT: 6-7 weeks
price: contact lab
Sanger sequencing of the UGT1A1 gene
method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Capillary (Sanger) 
Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain
TAT: 4-5 weeks
price: contact lab
Detection of the A(TA)7TAA allele in the UGT1A1 gene promotor
method(s): ◦ Repeat Expansion / Contraction 
Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain
TAT: 4 weeks
price: contact lab
UGT1A1 sequencing
method(s): ◦ Sequencing, Next Gen 
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA
TAT: 4 weeks
price: contact lab
UGT1A1 deletion/duplication
method(s): ◦ Del/Dup (CNV) 
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA
TAT: 2 weeks
price: contact lab
UGT1A1 genotyping for Gilbert syndrome
method(s): ◦ Genotyping (Microarray, Beads, etc.) 
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA
TAT: 1 week
price: contact lab
UGT1A1 genotyping for irinotecan dosing
method(s): ◦ Genotyping (Microarray, Beads, etc.) 
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA
TAT: 2-3 weeks
price: contact lab
UGT1A1 Gene Sequencing
method(s): ◦ Sequencing, Capillary (Sanger) 
Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany
Gilbert Syndrome
method(s): ◦ Genotyping (Microarray, Beads, etc.) ◦ Sequencing, Capillary (Sanger) 
Laboratories AGEL a.s. - Novy Jicin, Czech Republic
Crigler-Najjar Syndrome
method(s): ◦ Sequencing, Capillary (Sanger) 
Laboratories AGEL a.s. - Novy Jicin, Czech Republic
Crigler-Najjar Syndrome Types 1 and 2, Sequencing UGT1A1 Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
Gilbert Syndrome, Polymorphism UGT1A1 Gene
method(s): ◦ Microarray (CGH-Oligo, SNP, BAC) 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: 7-10 days
price: contact lab
Crigler-Najjar Syndrome
method(s): ◦ Genotyping (Microarray, Beads, etc.) 
Recombine - Livingston, NJ, USA
Gilbert syndrome (sequence analysis of UGT1A1 gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
Gilbert syndrome (TA insertion on UGT1A1 gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
Crigler Najjar syndrome types 1 and 2 (sequence analysis of UGT1A1 gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
TAT: 1-2 weeks
price: contact lab
UDP-Glucuronosyl Transferase 1A1 (UGT1A1), Full Gene Sequencing, Hyperbilirubinemia
method(s): ◦ Sequencing, Capillary (Sanger) 
Mayo Clinic - Minnesota, Personalized Genomics Laboratory - Rochester, MN, USA
TAT: 1-2 weeks
price: contact lab
UDP-Glucuronosyl Transferase 1A1 (UGT1A1), Full Gene Sequencing, Irinotecan Hypersensitivity
method(s): ◦ Sequencing, Capillary (Sanger) 
Mayo Clinic - Minnesota, Personalized Genomics Laboratory - Rochester, MN, USA
TAT: 1 week
price: contact lab
UDP-Glucuronosyl Transferase 1A1 TA Repeat Genotype, UGT1A1
method(s): ◦ Genotyping (Microarray, Beads, etc.) 
Mayo Clinic - Minnesota, Personalized Genomics Laboratory - Rochester, MN, USA
TAT: 1-2 weeks
price: contact lab
UDP-Glucuronosyl Transferase 1A1 (UGT1A1) Gene, Known Mutation
method(s): ◦ Sequencing, Capillary (Sanger) 
Mayo Clinic - Minnesota, Personalized Genomics Laboratory - Rochester, MN, USA
UGT1A1 TA polymorphism
method(s): ◦ Del/Dup (CNV) 
University of California, San Francisco, Molecular Diagnostics Laboratory - San Francisco, CA, USA
TAT: 1-2 weeks
price: contact lab
Crigler-Najjar Syndrome (UGT1A1 gene) Old Order Amish and Mennonite targeted mutation analysis
method(s): ◦ Genotyping (Microarray, Beads, etc.) 
DDC Clinic Molecular Diagnostics Laboratory - Middlefield, OH, USA
Hereditary Hemolytic Anemia Sequencing, 28 Genes
method(s): ◦ Sequencing, Next Gen 
ARUP Laboratories, Molecular Genetics Laboratory - Salt Lake City, UT, USA
TAT: 7-10 days
price: contact lab
NewbornDx
method(s): ◦ Sequencing, Next Gen 
Parabase Genomics - Boston, MA, USA
TAT: 4-6 weeks
price: contact lab
Somatic Tumor Panel
method(s): ◦ Sequencing, Next Gen 
CeGaT GmbH - Tübingen, Germany
Neonatal and Adult Cholestasis: Sequencing Panel
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen 
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada
Neonatal and Adult Cholestasis: Deletion/Duplication Panel
method(s): ◦ Del/Dup (CNV) 
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada
Gilbert syndrome
method(s): ◦ Genotyping (Microarray, Beads, etc.) 
GMDL Genica - Sofia, Bulgaria
UGT1A1 Promoter Region Testing for Irinotecan Therapy Hepatotoxicity
method(s): ◦ Genotyping (Microarray, Beads, etc.) 
GMDL Genica - Sofia, Bulgaria
UDP Glucuronosyltransferase 1A1 (UGT1A1) Genotyping
method(s): ◦ Genotyping (Microarray, Beads, etc.) 
ARUP Laboratories, Molecular Genetics Laboratory - Salt Lake City, UT, USA
TAT: 2-4 weeks
price: contact lab
Pain Syndromes (NextGen Sequencing Panel and Copy Number Analysis; 30 Genes)
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen 
MNG Laboratories (Medical Neurogenetics, LLC.) - Atlanta, GA, USA
TAT: 4 weeks
price: contact lab
UGT1A1 Deletion/duplication analysis
method(s): ◦ Del/Dup (CNV) 
Cincinnati Children's Hospital Medical Center, Molecular Genetics Laboratory - Cincinnati, OH, USA
TAT: 4-5 Weeks
price: contact lab
UGT1A1
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
Irinotecan toxicity (TA insertion on UGT1A1 gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
TAT: 4 weeks
price: contact lab
Crigler-Najjar Syndrome: gene UGT1A1
method(s): ◦ Sequencing, Capillary (Sanger) 
GenoMed-Diagnosticos de Medicina Molecular, SA - Lisboa, Portugal
TAT: 4 weeks
price: contact lab
Gilbert Syndrome: UGT1A1 gene
method(s): ◦ Sequencing, Capillary (Sanger) 
GenoMed-Diagnosticos de Medicina Molecular, SA - Lisboa, Portugal
TAT: 1 week
price: contact lab
Chemo DME Panel
method(s): ◦ Genotyping (Microarray, Beads, etc.) 
Castle Medical, LLC - Smyrna, GA, USA
TAT: 3-4 weeks
price: contact lab
Cholestasis Panel
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen 
Blueprint Genetics - Helsinki, Finland
TAT: 7-10 days
price: $249.00
OneOme RightMed pharmacogenomic test
method(s): ◦ Del/Dup (CNV) ◦ Genotyping (Microarray, Beads, etc.) 
OneOme - Minneapolis, MN, USA
TAT: 3-4 weeks
price: $690.00
Crigler-Najjar Syndrome and Gilbert Syndrome via the UGT1A1 Gene
method(s): ◦ Del/Dup (CNV) 
PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA
TAT: 2-3 weeks
price: $680.00
Crigler-Najjar Syndrome and Gilbert Syndrome via the UGT1A1 Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA
TAT: 4 weeks
price: contact lab
UGT1A1 Gene Sequencing
method(s): ◦ Sequencing, Next Gen 
Cincinnati Children's Hospital Medical Center, Molecular Genetics Laboratory - Cincinnati, OH, USA
TAT: 4-6 weeks
price: contact lab
UGT1A1 Gene Sequencing
method(s): ◦ Sequencing, Next Gen 
DDC Clinic Molecular Diagnostics Laboratory - Middlefield, OH, USA
Hyperbilirubinemia (Hyperbilirubinemia)
method(s): ◦ Sequencing, Next Gen 
Praxis fuer Humangenetik Wien - Vienna, Austria
TAT: ~2 weeks
price: contact lab
Gilbert syndrome
method(s): ◦ Sequencing, Capillary (Sanger) 
Centogene AG, Rare Disease Company - Rostock, Germany
Gilbert Syndrome, Sequencing UGT1A1 Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: ~2 weeks
price: contact lab
Crigler-Najjar syndrome, type 1
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany
TAT: ~2 weeks
price: contact lab
Crigler-Najjar syndrome, type 2
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany
TAT: ~2 weeks
price: contact lab
Hyperbilirubinemia, familial transient neonatal
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany