Version 2.77

Part Description

LP61778-4   FLT3 gene
The FLT3 gene (fms-related tyrosine kinase 3) [HGNC Gene ID:3765] is located on chromosome 13q12. This gene encodes a class III receptor tyrosine kinase that regulates hematopoiesis. This receptor is activated by binding of the fms-related tyrosine kinase 3 ligand to the extracellular domain, which induces homodimer formation in the plasma membrane leading to autophosphorylation of the receptor. The activated receptor kinase subsequently phosphorylates and activates multiple cytoplasmic effector molecules in pathways involved in apoptosis, proliferation, and differentiation of hematopoietic cells in bone marrow. Mutations that result in the constitutive activation of this receptor result in acute myeloid leukemia and acute lymphoblastic leukemia. [provided by RefSeq, Jan 2015] [NCBI Gene ID:2322] FLT3 mutations occur in approximately 1/3 of patients with AML. About 70% are internal tandem duplications, and the rest are due to variants in the tyrosine kinase domain of FLT3, primarily at Asp835 (D835). PMID: 17124058 Source: Regenstrief LOINC

Fully-Specified Name

Component
FLT3 gene targeted mutation analysis
Property
Find
Time
Pt
System
Bone mar
Scale
Doc
Method
Molgen

Additional Names

Short Name
FLT3 gene Mut Anl Mar
Display Name
FLT3 gene targeted mutation analysis Molgen Doc (BM)
Consumer Name Alpha Get Info
FLT3 gene targeted mutation analysis, Bone marrow

Basic Attributes

Class
MOLPATH.MUT
Type
Laboratory
First Released
Version 2.27
Last Updated
Version 2.73
Change Reason
Based on LOINC Committee review (June 2016), "targeted" was added to the Component to clarify that this test is looking for a specific set of mutations as described in the LOINC User Guide under the Molecular Genetics section.; Based on LOINC Committee review (June 2019), updated the Property from "Prid" to "Find" and Scale from "Nar" to "Doc" to align with the current LOINC model for naming collections of information reported in narrative and/or structured formats.
Order vs. Observation
Both
Common Test Rank Get Info
17255

Language Variants Get Info

Tag Language Translation
es-ES Spanish (Spain) Gen FLT3 Analisis de mutaciones:Hallazgo:Punto temporal:Médula ósea:Doc:Genética molecular
es-MX Spanish (Mexico) Análisis de mutaciones dirigidas al gen FLT3:Hallazgo:Punto temporal:Médula ósea:Documento:Genética molecular
fr-FR French (France) FLT3 gène mutation cible trouvée:Recherche:Ponctuel:Moelle osseuse:Document:Biologie moléculaire
it-IT Italian (Italy) FLT3, gene analisi di mutazione mirata:Osservazione:Pt:Mid oss:Doc:Molgen
Synonyms: Gene FLT3 Genetica molecolare Midollo osseo Mutazione genica Osservazione Patologia molecolare Punto nel tempo (episodio)
nl-NL Dutch (Netherlands) FLT3-gen doelgerichte mutatie-analyse:bevinding:moment:beenmerg:document:moleculair genetisch onderzoek
Synonyms: FLT3 gen molgen targeted
pt-BR Portuguese (Brazil) FLT3 análise de mutação do gene:#N/A:Pt:MedOssea:Nar:Genética molecular
Synonyms: FLK2; STK-1; STK1; FL cytokine receptor precursor; Stem cell tyrosine kinase 1; fms-related tyrosine kinase 3; Identity or presence; Point in time; Random; BM; Bone marrow; BON; Narrative; Report; PCR; Molecular genetics; Mut Anal; Mutations; MOLPATH.MUTATIONS; MOLPATH.MUTATIONS; Molecular pathology
ru-RU Russian (Russian Federation) FLT3 ген исследование на мутацию:Находка:ТчкВрм:Костный мозг:Док:МолГен
Synonyms: Документ Точка во времени;Момент
tr-TR Turkish (Turkey) FLT3 geni Mutasyon analizi:Bulgu:Zmlı:Kem il:Dokm:Molgen
zh-CN Chinese (China) FLT3 基因 突变分析:发现:时间点:骨髓:文档型:分子遗传学类实验室方法
Synonyms: FL 细胞因子受体前体;FLK2;fms-相关性酪氨酸激酶 3;STK1;STK-1;干细胞酪氨酸激酶 1 临床文档型;临床文档;文档;文书;医疗文书;临床医疗文书 分子病理学.基因突变;分子病理学.突变;分子病理学试验.基因突变;分子病理学试验.突变;分子病理学试验类.突变;基因突变;突变 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 发现是一个原子型临床观察指标,并不是作为印象的概括陈述。体格检查、病史、系统检查及其他此类观察指标的属性均为发现。它们的标尺对于编码型发现可能是名义型,而对于叙述型文本之中所报告的发现,则可能是叙述型。;发现物;所见;结果;结论 基因突变分析 时刻;随机;随意;瞬间 遗传基因;遗传因子;吉恩;生物基因 骨骼;骨头 髓

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=54447-8