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Part Description

LP19829-8   t(1;19)(q23.3;p13.3)(PBX1,TCF3)
Chromosomal translocation t(1;19)(q23.3;p13.3) PBX1/TCF3 is caused by a breakpoint in 19p13.3 and occurs in two different forms: 1) a balanced form found in one fourth of cases with a der(1) and a der(19) and 2) an unbalanced form found in 3/4 cases with 2 normal chromosomes 1, a der(19), and 1 normal chromosome 19. This translocation is mostly found in acute lymphoblastic leukemia (ALL), L1/L2 type, as well as L3-like ALL, T-lineage ALL (T-ALL), non-Hodgkin lymphomas (NHL), and acute myeloid leukemias (AML).[Atlas Genetics Oncology:t0119ID1048] Source: Regenstrief LOINC, t(1;19)(q23;p13) TCF3/PBX1

LOINC Names Get Info

Fully-Specified Name
t(1;19)(q23.3;p13.3)(PBX1,TCF3) fusion transcript:Arb:Pt:Bld/Tiss:Ord:Molgen
Long Common Name
t(1;19)(q23.3;p13.3)(PBX1,TCF3) fusion transcript [Presence] in Blood or Tissue by Molecular genetics method
Short Name
t(1;19)(PBX1,TCF3) Bld/T Ql
Display Name
t(1;19)(q23.3;p13.3)(PBX1,TCF3) fusion transcript Molgen Ql (Bld/Tiss)
Consumer Name Alpha Get Info
t(1;19)(q23.3;p13.3)(PBX1,TCF3) fusion transcript analysis, Blood or tissue specimen

Part Model Get Info

  • Component
    t(1;19)(q23.3;p13.3)(PBX1,TCF3) fusion transcript
    LP229723-4
    • Analyte
      t(1;19)(q23.3;p13.3)(PBX1,TCF3) fusion transcript
      LP229723-4
      • Component Numerator
        t(1;19)(q23.3;p13.3)(PBX1,TCF3) fusion transcript
        LP229723-4
        • Component Numerator Core
          t(1;19)(q23.3;p13.3)(PBX1,TCF3)
          LP19829-8
        • Component Numerator Core Suffix
          fusion transcript
          LP150217-0
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    Arb
    LP6781-1
  • Time
    Pt
    LP6960-1
  • System
    Bld/Tiss
    LP7061-7
    • System Core
      Bld/Tiss
      LP7061-7
    • Super System
      NULL
       
  • Scale
    Ord
    LP7751-3
  • Method
    Molgen
    LP6404-0

Basic Attributes

Class
MOLPATH.TRNLOC
Type
Laboratory
First Released
Version 1.0m
Last Updated
Version 2.73 (MIN)
Change Reason
Updated Component part to harmonize with ISCN guidelines and current LOINC nomenclature.
Order vs. Observation
Observation
Common Test Rank Get Info
17607

Member of these Panels

LOINCLong Common Name
72103-5Acute and chronic leukemia fusion transcript panel - Blood or Tissue by Molecular genetics method

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Fúzní transkript t(1;19)(q23.3;p13.3)(PBX1,TCF3):Arbitrární:Časový bod:Krev/tkáň:Ordinální:Molekulární genetika
el-GRGreek (Greece)t(1;19)(q23.3;p13.3)(PBX1,TCF3) μεταγραφή συγχώνευσης:Arb:Pt:Αίμα/Ιστός:Ord:Μοριακή γενετική
Synonyms: Arb MOLPATH MOLPATH.TRNLOC Ord Pt t(1;19)(q23.3;p13.3)(PBX1,TCF3) Αίμα Αίμα/Ιστός Ιστός μεταγραφή συγχώνευσης Μοριακή γενετική
es-ARSpanish (Argentina)translocación del gen T(1,19)(PBX1,TCF3):arbitrario:punto en el tiempo:sangre entera/tejido:ordinal:genética molecular
es-ESSpanish (Spain)t(1;19)(q23.3;p13.3)(PBX1,TCF3) Tránscritos de fusión:Arbitrario:Punto temporal:Sangre o tejido:Ord:Genética molecular
es-MXSpanish (Mexico)t (1; 19) (q23.3; p13.3) (PBX1, TCF3) transcripción de fusión:Arbitrario:Punto temporal:Sangre o tejido:Ordinal:Genética molecular
fr-FRFrench (France)t(1;19)(q23.3;p13.3)(PBX1,TCF3) transcript de fusion:Arbitraire:Ponctuel:Sang/Tissu:Qualitatif:Biologie moléculaire
fr-CAFrench (Canada)t(1;19)(q23.3;p13.3)(PBX1,TCF3) transcrit de fusion:Arbitraire:Temps ponctuel:Sang/Tissu:Ordinal:Molgen
it-ITItalian (Italy)t(1,19)(q23.3,p13.3)(PBX1,TCF3), trascritto di fusione:Arb:Pt:Sangue/Tess:Ord:Molgen
Synonyms: Arbitrario Genetica molecolare Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & Strisci Traslocazione genetica
ko-KRKorean (Korea, Republic Of)t(1,19)(PBX1,TCF3) 유전자 전위:임의적분:검사시점:전혈/조직:순위척도:분자유전
nl-NLDutch (Netherlands)t(1;19)(q23.3;p13.3)(PBX1,TCF3) fusietranscript:aanwezigheid:moment:bloed of weefsel:ordinaal:moleculair genetisch onderzoek
Synonyms: molgen
pt-BRPortuguese (Brazil)t(1,19)(PBX1,TCF3) translocação do gene:Arb:Pt:Sg/Tecido:Ord:Genética molecular
Synonyms: Arbitrary; Point in time; Random; Bld/T; Tissue; Bld/T; Blood; WB; Whole blood; Ql; Ordinal; QL; Qualitative; Qual; Screen; PCR; Molecular genetics; E2A Immunoglobulin enhancer binding factors E12/E47; ITF1; Immunoglobulin transcription factor 1; Transcription factor 3; Acute lymphocytic leukemia; ALL; t(1,19)(q23,p13); T prime; PBXP1; Pre-B cell leukemia transcription factor-1; I; MOLPATH.TRANSLOCATION; MOLPATH.TRANSLOCATION; Molecular pathology
ru-RURussian (Russian Federation)t(1;19)(q23.3;p13.3)(PBX1,TCF3) слияния транскрипт:Произв:ТчкВрм:Кр/Тк:Пор:МолГен
Synonyms: Кровь Кровь или Ткань Порядковый Произвольный Ткань и мазки Точка во времени;Момент химерная РНК, закодированная слитым геном
tr-TRTurkish (Turkey)t(1;19)(q23.3;p13.3)(PBX1,TCF3) füzyon transkript:Sç:Zmlı:Kan/Dk:Srl:Molgen
zh-CNChinese (China)t(1;19)(q23.3;p13.3)(PBX1,TCF3) 融合转录物:任意型:时间点:全血/组织:序数型:分子遗传学类实验室方法
Synonyms: Ⅰ E2A 免疫球蛋白增强子结合因子 E12/E47 E2A 免疫球蛋白增强子结合因子 E12/E47（E2A Immunoglobulin enhancer binding factors E12/E47） I ITF1 PBXP1 T(1,19)(PBX1,TCF3) 基因易位;T(1,19)(PBX1,TCF3) 易位 任意;任意的;人工型 依次型;分类顺序型;定性的;序数型（或称等级型）;性质上的;有序型;有序性分类应答;有序性分类结果;秩次型;等级型;筛查;顺序型 免疫球蛋白转录因子 1 免疫球蛋白转录因子 1（Immunoglobulin transcription factor 1，ITF1） 全血或组织;血液/组织;血液或组织 分子病理学.基因易位;分子病理学.易位;分子病理学试验.基因易位;分子病理学试验.易位;分子病理学试验类.易位;基因易位 分子病理学;分子病理学试验 分子遗传学;分子遗传学方法;分子遗传学类方法;分子遗传学类检验方法;包括 RFL、PCR 及其他方法在内，用于在分子基础上检测遗传属性的方法的大类;聚合酶链反应;聚合酶链式反应 前 B 细胞白血病转录因子-1 前 B-细胞白血病转录因子-1 前 B-细胞白血病转录因子-1（Pre-B cell leukemia transcription factor-1，PBX1，PBXP1） 时刻;随机;随意;瞬间 未作说明的组织;组织;组织 & 涂片 融合转录物（转录本、转录产物、转录子、转录）;融合基因转录本;融合转录 血;血液 转录因子 3 转录因子 3（Transcription factor 3，TCF3）

LOINC Terminology Service (API) using HL7® FHIR® Get Info

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=21800-8