AutoICD API

70282-9

Laboratory

t(9;12)(q34.1;p13)(ABL1,ETV6) fusion transcript [Presence] in Blood or Tissue by Molecular genetics method

Definition

This term is used to identify a leukemia causing chromosomal translocation resulting in a gene fusion between ABL1 (9q34) and ETV6 (12p13) genes. The term was created for (but not limited to) DNA Technology's HemaVision HV01-28N kit, a qualitative in vitro diagnostic test for 28 leukemia causing chromosomal alterations including more than 80 breakpoints plus associated mRNA splice variants. Reverse transcription followed by multiplex nested polymerase chain reactions (RT-PCR) and agarose gel electrophoresis are used to identify gene fusions caused by chromosomal translocations, gene deletions or inversions. Testing information is useful for predicting development of the disease and selection of treatment.

LOINC 6-Axis Classification

Component

t(9;12)(q34.1;p13)(ABL1,ETV6) fusion transcript

Property

Arb

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Ord

Method Type

Molgen

Details

Class

MOLPATH.TRNLOC

Order/Observation

Both

Short Name

t(9;12)(ABL1,ETV6) Bld/T Ql

Display Name

t(9;12)(q34.1;p13)(ABL1,ETV6) fusion transcript Molgen Ql (Bld/Tiss)

Related Names

ABLArbitraryBloodDNAets variant gene 6gene fusiongene translocationGeneticsHeredityHeritableInheritedJTK7Molecular geneticsMolecular pathologyMOLPATHMOLPATH.TRANSLOCATIONOrdinalp150PCRPoint in timeQLQualQualitativeRandomRNAScreenT primet(912)(ABL1,ETV6)TELTel oncogeneTEL1TissueTissue, unspecifiedtranslocationTranslocation ets leukemiav-abl Abelson murine leukemia viral oncogene homolog 1WBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 70282-9?

LOINC code 70282-9 identifies "t(9;12)(q34.1;p13)(ABL1,ETV6) fusion transcript [Presence] in Blood or Tissue by Molecular genetics method". This term is used to identify a leukemia causing chromosomal translocation resulting in a gene fusion between ABL1 (9q34) and ETV6 (12p13) genes. The term was created for (but not limited to) DNA Technology's HemaVision HV01-28N kit, a qualitative in vitro diagnostic test for 28 leukemia causing chromosomal alterations including more than 80 breakpoints plus associated mRNA splice variants. Reverse transcription followed by multiplex nested polymerase chain reactions (RT-PCR) and agarose gel electrophoresis are used to identify gene fusions caused by chromosomal translocations, gene deletions or inversions. Testing information is useful for predicting development of the disease and selection of treatment.

What does 70282-9 measure?

This code measures t(9;12)(q34.1;p13)(ABL1,ETV6) fusion transcript in Bld/Tiss. It belongs to the MOLPATH.TRNLOC 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.