AutoICD API

72886-5

Laboratory

CYP2D6 gene and CYP2C19 gene targeted mutation analysis panel - Blood or Tissue by Molecular genetics method

Definition

CYP2D6 and CYP2C19 cytochrome P450 genes play a major role in the metabolism of many widely prescribed drugs, including anti-depressants, anti-psychotics, anti-epileptics, proton pump inhibitors, and beta-blockers. The CYP2D6 gene has at least 70 allelic variants resulting in four phenotypic types: poor metabolizers with gene inactivation of both alleles, intermediate metabolizers with one reduced activity allele and one null allele, extensive metabolizers with at least one functional allele, and ultra-rapid metabolizers with excess enzymatic activity due to multiple copies of functional alleles from gene duplication. The CYP2C19 gene has two major variant alleles that result in enzyme deficiency. This panel term is created for, but not limited to, Roche Diagnostics' AmpliChip CYP450 assay, which detects 29 polymorphisms in the 2D6 and 2 polymorphisms in the 2C19 gene, as well as gene duplications and deletions.

LOINC 6-Axis Classification

Component

CYP2D6 gene & CYP2C19 gene targeted mutation analysis panel

Property

-

Time Aspect

Pt

System

Bld/Tiss

Scale Type

-

Method Type

Molgen

Details

Class

PANEL.MOLPATH.PHARMG

Order/Observation

Order

Short Name

CYP2D6+CYP2C19 pnl Bld/T

Display Name

CYP2D6 gene and CYP2C19 gene targeted mutation analysis panel Molgen (Bld/Tiss)

Related Names

BloodCPCJCPD6CYP2CCYP2DCYP2D@CYP2D6+CYP2C19CYP2D6+CYP2C19 pnlCYP2D7APCYP2D7BPCYP2D7P2CYP2D8P2CYP2DL1CYPIIC17CYPIIC19CYPIID6Cytochrome p450cytochrome P-450 II Ccytochrome P450, family 2, subfamily C, polypeptide 19cytochrome P450, family 2, subfamily D, polypeptide 6Debrisoquine hydroxylation geneHGNC:2629Molecular geneticsMolecular pathologyMOLPATHMOLPATH.PHARMGMutMutationsP450C2CP450C2DP450DB1P450-DB1P450IIC19PanPanel.molpathPanel.molpath.pharmgPanlPCRPnlPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 72886-5?

LOINC code 72886-5 identifies "CYP2D6 gene and CYP2C19 gene targeted mutation analysis panel - Blood or Tissue by Molecular genetics method". CYP2D6 and CYP2C19 cytochrome P450 genes play a major role in the metabolism of many widely prescribed drugs, including anti-depressants, anti-psychotics, anti-epileptics, proton pump inhibitors, and beta-blockers. The CYP2D6 gene has at least 70 allelic variants resulting in four phenotypic types: poor metabolizers with gene inactivation of both alleles, intermediate metabolizers with one reduced activity allele and one null allele, extensive metabolizers with at least one functional allele, and ultra-rapid metabolizers with excess enzymatic activity due to multiple copies of functional alleles from gene duplication. The CYP2C19 gene has two major variant alleles that result in enzyme deficiency. This panel term is created for, but not limited to, Roche Diagnostics' AmpliChip CYP450 assay, which detects 29 polymorphisms in the 2D6 and 2 polymorphisms in the 2C19 gene, as well as gene duplications and deletions.

What does 72886-5 measure?

This code measures CYP2D6 gene & CYP2C19 gene targeted mutation analysis panel in Bld/Tiss. It belongs to the PANEL.MOLPATH.PHARMG class in the LOINC classification.

What is LOINC?

LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.