LOINC Code 70276-1: t(1;11)(p32;q23)(EPS15,MLL) fusion transcript Molgen Ql (Bld/Tiss)
70276-1 is a LOINC code used to identify t(1;11)(p32;q23)(EPS15,MLL) fusion transcript Molgen Ql (Bld/Tiss) in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component t(1;11)(p32;q23)(EPS15,MLL) fusion transcript. It is commonly used with the system or sample type Bld/Tiss.
What is this code?
LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component t(1;11)(p32;q23)(EPS15,MLL) fusion transcript. It is commonly used with the system or sample type Bld/Tiss.
When is it used?
- Used in lab systems, EHRs, and clinical data exchange.
- May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
- Status: ACTIVE
- Order vs observation: Both
- Method: Molgen
What it does not mean
- The code identifies the observation or test, not the actual result.
Key facts
- t(1;11)(p32;q23)(EPS15,MLL) fusion transcript [Presence] in Blood or Tissue by Molecular genetics method
- t(1;11)(p32;q23)(EPS15,MLL) fusion transcript
- This term is used to identify a leukemia causing chromosomal translocation resulting in a gene fusion between EPS15 (1p32) and MLL (11q23) 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.
- 1p32; AF-1P; ALL1; ALL-1; Arbitrary; Blood; DNA; epidermal growth factor receptor pathway substrate 15; gene fusion; gene translocation; Genetics; Heredity; Heritable; HRX; HTRX; HTRX1; i; Inherited; MLLT5; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.TRANSLOCATION; myeloid/lymphoid or mixed-lineage leukemia (trithorax (Drosophila) homolog); Ordinal; PCR; Point in time; QL; Qual; Qualitative; Random; RNA; Screen; T prime; t(1;11)(EPS15,MLL); Tissue; Tissue, unspecified; translocation; TRX1; WB; Whole blood; Whole blood or Tissue
Where you may see this code
You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.
Common synonyms
Frequently asked questions
About this content
This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.