82904-4
t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript [Presence] in Bone marrow by Molecular genetics method
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Part Description
LP150238-6 t(9;22)(q34.1;q11)(ABL1,BCR)
Chronic myelogenous leukemia (CML), acute lymphoblastic leukemia (ALL), and acute myeloid leukemia (AML) are associated with the fusion of the breakpoint cluster gene (BCR) at chromosome 22q11 to the Abelson gene (ABL1) at chromosome 9q23. The t(9;22)(BCR-ABL1) gene translocation leads to the cytogenetic finding known as the Philadelphia chromsome (Ph'). Various breakpoints within the BCR and ABL1 genes have been described. Most cases of CML are due to a fusion of BCR exon 13 (e13 or b2) or BCR exon 14 (e14 or b3) to the ABL exon 2 (a2). The b2a2 (e13a2) and b3a2 (e14a2) fused transcripts, also known as major break points, produce a 210-kDa protein (p210). The fused transcript resulting in a 190-kDa protein (e1a2 or less common e1a3), also known as minor break points, is found in approximately 75% of childhood ALL patients and 50% of adult ALL patients. Other rarely reported fused transcripts include e6a2, e19a2 (p230), e13a3, and e14a3.
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript
- Property
- PrThr
- Time
- Pt
- System
- Bone mar
- Scale
- Ord
- Method
- Molgen
Additional Names
- Short Name
- t(9;22)(ABL1,BCR) Mar Ql
- Display Name
- t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript Molgen Ql (BM)
- Consumer Name Alpha Get Info
- t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript analysis, Bone marrow
Example Answer List: LL3950-4
Source: Regenstrief LOINCAnswer | Code | Score | Answer ID |
---|---|---|---|
PresentCopyright http://snomed.info/sct ID:52101004 Present (qualifier value) | LA9633-4 | ||
AbsentCopyright http://snomed.info/sct ID:2667000 Absent (qualifier value) | LA9634-2 |
Basic Attributes
- Class
- MOLPATH.TRNLOC
- Type
- Laboratory
- First Released
- Version 2.58
- Last Updated
- Version 2.58
- Order vs. Observation
- Both
Language Variants Get Info
Tag | Language | Translation |
---|---|---|
es-ES | Spanish (Spain) | t(9; |
es-MX | Spanish (Mexico) | t (9; |
fr-FR | French (France) | t(9; |
fr-CA | French (Canada) | t(9; |
it-IT | Italian (Italy) | t(9; Synonyms: Genetica molecolare Midollo osseo Patologia molecolare Presenza o Soglia Punto nel tempo (episodio) Traslocazione genetica |
nl-NL | Dutch (Netherlands) | t(9; Synonyms: molgen |
ru-RU | Russian (Russian Federation) | t(9; Synonyms: Порядковый Точка во времени; |
tr-TR | Turkish (Turkey) | t(9; Synonyms: Mevcut |
zh-CN | Chinese (China) | t(9; Synonyms: ABL CML JTK7 p150 v-abl Abelson murine leukemia viral oncogene homolog 1 v-abl Abelson 小鼠白血病病毒癌基因同源体 1 v-abl Abelson 小鼠白血病病毒肿瘤基因同源体 1 v-abl Abelson 小鼠白血病病毒致癌基因同源体 1 v-abl Abelson 鼠科动物白血病病毒致癌基因同源体 1 v-abl Abelson 鼠科白血病病毒致癌基因同源体 1 依次型; |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=82904-4
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Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright