UGT1A1 gene TA repeats [Genotype] in Blood or Tissue by Molecular genetics method Nominal   95143-4

LOINC Code


LOINC code95143-4
nameUGT1A1 gene TA repeats [Genotype] in Blood or Tissue by Molecular genetics method Nominal
descriptionThe patient's genotype (e.g. TA5/TA7) for the TA repeat variant within the UGT1A1 gene. Variants include TA5 or *36: c.−41_-40delTA (g.234668893_234668894), TA7 or *28: c.−41_-40dupTA (g.234668893_234668894), and TA8 or *37: c.−43_-40dupTATA (g. 234668891_234668894). Testing is performed to screen for variants associated with increased risk of adverse drug reactions when taking UGT1A1-metabolized drugs, including pazopanib, nilotinib, atazanavir, and belinostat. Patient's homozygosity for the TA7 promoter variant (*28) have reduced UGT1A1 activity (about 30% to 50%) compared to normal.[PMID: 7565971]
statusACTIVE

Fully-Specified Name

componentUGT1A1 gene.TA repeats
propertyGeno  =  Genotype
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
systemBld/Tiss
    Bld  =  Whole blood
    Tiss  =  Tissue, unspecified
scaleNom  =  Nominal:  Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody.
methodMolgen  =  Molecular Genetics:  General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods.

Additional Names

short nameUGT1A1 TA Geno Bld/T

Basic Attributes

classMOLPATH.PHARMG
type1  Laboratory
order vs. observationBoth

Associated Observations

LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations.

History/Usage

first released
last updated2.68
last change typeADD  - added

Related Names

BILIQTL1
Blood
Crigler-Najjar syndrome, type I
Genetics
Gilbert Syndrome
GNT1
Heredity
Heritable
HUG-BR1
Inherited
Ma2
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.PHARMG
Nominal
PCR
Point in time
Random
Repeat
Tissue
Tissue, unspecified
UDP glucuronosyltransferase 1 family, polypeptide A1
UDP glycosyltransferase 1 family, polypeptide A1 gene
UDPGT
UDPGT 1-1
UGT1
UGT1A
UGT1A1 TA
UGT1A5
WB
Whole blood
Whole blood or Tissue

Copyright © 2023 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2023, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.