Cost 
$875.00
TAT 
4 weeks
CPT Code 
81403
81404
Test Code 
1297
Test Methods 
Sequencing
Deletion/Duplication analysis
Specimen Types Accepted 
Blood
Saliva
Buccal
Cultured Cells
Extracted DNA
Genes 
Notes 
UGT1A1 analysis will also detect the UGT1A1*28 variant in the promoter region of the UGT1A1 gene, if present. This variant, when present in the homozygous state, is associated with Gilbert syndrome.

Crigler-Najjar syndromes (CN) are inborn disorders of the liver metabolism of bilirubin characterized by non-hemolytic unconjugated hyperbilirubinemia. CN are classified into two types based on the bilirubin levels, the presence of kernicterus and the reduction of the bilirubin levels upon administration of Phenobarbital or other enzyme-inducing agents.

Mutations in the UGT1A1 gene [OMIM #191740] have been identified in patients with CN. The UGT1A1 gene maps to 2q37.1. It has 4 coding exons, and to date missense, nonsense, frameshift and splice site mutations, and small insertions and deletions have been described