21819-8
t(8;21)(q22;q22.3)(RUNX1T1,RUNX1) fusion transcript [Presence] in Blood or Tissue by Molecular genetics method
Active
Part Description
LP19847-0 t(8;21)(q22;q22.3)(RUNX1T1,RUNX1)
Translocation (8;21) resulting in a fused transcript between RUNX1T1 (also known as ETO) and RUNX1 genes is one of the most common chromosomal translocations found in acute myeloid leukemia (AML). The RUNX1T1-RUNX1 fusion transcript is found in approximately 12% of all AML patients. RUNX1 is a transcription factor that regulates critical processes in many aspects of hematopoiesis and is essential in defining the final hematopoietic stem cell. It is involved in many forms of chromosomal translocations in leukemia. In addition, many hematological diseases have been associated with mutations in RUNX1. PMID: 22201794
Source: Regenstrief LOINC, PMID: 22201794
Fully-Specified Name
- Component
- t(8;21)(q22;q22.3)(RUNX1T1,RUNX1) fusion transcript
- Property
- Arb
- Time
- Pt
- System
- Bld/Tiss
- Scale
- Ord
- Method
- Molgen
Additional Names
- Short Name
- t(8;21)(RUNX1T1,RUNX1) Bld/T Ql
- Display Name
- t(8;21)(q22;q22.3)(RUNX1T1,RUNX1) fusion transcript Molgen Ql (Bld/Tiss)
- Consumer Name Alpha Get Info
- t(8;21)(q22;q22.3)(RUNX1T1,RUNX1) fusion transcript analysis, Blood or tissue specimen
Basic Attributes
- Class
- MOLPATH.TRNLOC
- Type
- Laboratory
- First Released
- Version 1.0m
- Last Updated
- Version 2.73
- Change Reason
- Changed gene names CBFA2T1 to RUNX1T1 and CBFA2 to RUNX1, the recommended gene names by the HUGO Gene Nomenclature Committee (HGNC). Updated Component part to harmonize with ISCN guidelines and current LOINC nomenclature.
- Order vs. Observation
- Both
- Common Test Rank Get Info
- 5876
Member of these Panels
LOINC | Long Common Name |
---|---|
72103-5 | Acute and chronic leukemia fusion transcript panel - Blood or Tissue by Molecular genetics method |
Language Variants Get Info
Tag | Language | Translation |
---|---|---|
de-AT | German (Austria) | Synonyms: Translokation (8,21) |
es-AR | Spanish (Argentina) | translocación del gen T(8,21)(CBFA2T1,CBFA2): |
es-ES | Spanish (Spain) | t(8; |
es-MX | Spanish (Mexico) | t (8; |
fr-FR | French (France) | t(8; |
fr-CA | French (Canada) | t(8; |
it-IT | Italian (Italy) | t(8; Synonyms: Arbitrario Genetica molecolare Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & |
ko-KR | Korean (Korea, Republic Of) | t(8,21)(CBFA2T1,CBFA2) 유전자 전위: |
nl-NL | Dutch (Netherlands) | t(8; Synonyms: molgen |
pt-BR | Portuguese (Brazil) | t(8,21)(CBFA2T1,CBFA2) translocação do gene: Synonyms: Arbitrary; |
ru-RU | Russian (Russian Federation) | t(8; Synonyms: Кровь Кровь или Ткань Порядковый Произвольный Ткань и мазки Точка во времени; |
tr-TR | Turkish (Turkey) | t(8; |
zh-CN | Chinese (China) | t(8; Synonyms: AML1 CDR ETO MGC2796 MTG8 RUNX1T1 T(8,21)(CBFA2T1,CBFA2) 基因易位; |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
Requests to this service require a free LOINC username and password. Below is a sample of the possible capabilities. See the LOINC Terminology Service documentation for more information.
- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=21819-8
LOINC Copyright
Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright