72881-6

LOINC 2.82

UGT2B15 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

UGT2B15 Mut Anl Bld/T

Definition

  • A patient's genotype for the UGT2B15 gene is typically reported as *A/*B where A is the allele from one chromosome and B is the allele from the other chromosome. The genotype is determined by the analysis of specific single nucleotide polymorphisms (SNPs) within the gene by various molecular techniques, including PCR and microarray. In some cases, SNP results are analyzed by bioinformatics computer software to determine a patient's overall genotype.

Component

  • UGT2B15 gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.PHARMG

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • Blood; Genetics; Heredity; Heritable; HLUG4; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.PHARMG; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; Random; Tissue; Tissue, unspecified; UDP glucuronosyltransferase 2 family, polypeptide B15; UDPGT 2B8; UDPGT2B15; UDPGTH3; UGT2B8; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • Genetics
  • Heredity
  • Heritable
  • HLUG4
  • Identity or presence
  • Inherited
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.PHARMG
  • Mut
  • Mut Anl
  • Mutations
  • Nominal
  • PCR
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • UDP glucuronosyltransferase 2 family, polypeptide B15
  • UDPGT 2B8
  • UDPGT2B15
  • UDPGTH3
  • UGT2B15 gene targeted mutation analysis
  • UGT2B8
  • WB
  • Whole blood
  • Whole blood or Tissue