Version 2.78

Part Description

LP35583-1   MAPT gene
The MAPT gene (microtubule-associated protein tau) [HGNC Gene ID:6893] is located on chromosome 17q21.1. This gene encodes the microtubule-associated protein tau (MAPT) whose transcript undergoes complex, regulated alternative splicing, giving rise to several mRNA species. MAPT transcripts are differentially expressed in the nervous system, depending on stage of neuronal maturation and neuron type. MAPT gene mutations have been associated with several neurodegenerative disorders such as Alzheimer's disease, Pick's disease, frontotemporal dementia, cortico-basal degeneration and progressive supranuclear palsy. [provided by RefSeq, Jul 2008] [NCBI Gene ID:4137] Source: National Center for Biotechnology Information (NCBI) Gene

Fully-Specified Name

Component
MAPT gene targeted mutation analysis
Property
Prid
Time
Pt
System
Bld/Tiss
Scale
Nom
Method
Molgen

Additional Names

Long Common Name
MAPT gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
Short Name
MAPT gene Mut Anl Bld/T
Display Name
MAPT gene targeted mutation analysis Molgen Nom (Bld/Tiss)
Consumer Name Alpha Get Info
MAPT gene targeted mutation analysis, Blood or tissue specimen

Basic Attributes

Class
MOLPATH.MUT
Type
Laboratory
First Released
Version 2.15
Last Updated
Version 2.63
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.
Order vs. Observation
Both

Language Variants Get Info

Tag Language Translation
es-ES Spanish (Spain) Gen MAPT gene Analisis de mutaciones:Presencia o identidad:Punto temporal:Sangre o tejido:Nom:Genética molecular
es-MX Spanish (Mexico) Análisis de mutaciones dirigidas al gen MAPT:Presencia o identidad:Punto temporal:Sangre o tejido:Nominal:Genética molecular
fr-FR French (France) MAPT gène mutation cible trouvée:Identification:Ponctuel:Sang/Tissu:Résultat nominal:Biologie moléculaire
it-IT Italian (Italy) MAPT, gene analisi di mutazione mirata:Prid:Pt:Sangue/Tess:Nom:Molgen
Synonyms: Gene MAPT Genetica molecolare Mutazione genica Patologia molecolare Presenza o Identità Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & Strisci
ko-KR Korean (Korea, Republic Of) MAPT 유전자 돌연변이 분석:존재:검사시점:전혈/조직:명칭결과:분자유전
nl-NL Dutch (Netherlands) MAPT-gen doelgerichte mutatie-analyse:identificator:moment:bloed of weefsel:nominaal:moleculair genetisch onderzoek
Synonyms: MAPT gen molgen targeted
pt-BR Portuguese (Brazil) MAPT análise de mutação genética:Ident:Pt:Sg/Tecido:Nom:Genética molecular
Synonyms: DDPAC; FLJ31424; FTDP-17; MAPTL; MSTD; MTBT1; MTBT2; TAU gene; G protein beta1/gamma2 subunit-interacting factor 1; Disinhibition-dementia-Parkinsonism-amyotrophy complex; Microtubule-associated protein tau; Identity or presence; Point in time; Random; Bld/T; Tissue; Bld/T; Blood; WB; Whole blood; Nominal; PCR; Molecular genetics; Mut Anal; Mutations; MOLPATH.MUTATIONS; MOLPATH.MUTATIONS; Molecular pathology
ru-RU Russian (Russian Federation) MAPT ген исследование на мутацию:ПрИд:ТчкВрм:Кр/Тк:Ном:МолГен
Synonyms: Кровь Кровь или Ткань Номинальный;Именной Присутствие или Идентификация Ткань и мазки Точка во времени;Момент
tr-TR Turkish (Turkey) MAPT geni Mutasyon analizi:MevcKimlik:Zmlı:Kan/Dk:Snf:Molgen
zh-CN Chinese (China) MAPT 基因 突变分析:存在与否或特征标识:时间点:全血/组织:名义型:分子遗传学类实验室方法
Synonyms: DDPAC;FLJ31424;FTDP-17;G蛋白 beta1/gamma2 亚单位-交互因子 1;G蛋白 β1/γ2 亚单位-交互因子 1;MAPTL;MSTD;MTBT1;MTBT2;TAU 基因;微管相关蛋白 tau;抑制解除-痴呆-帕金森病-肌肉萎缩复合体;抑制解除-痴呆-帕金森病-肌萎缩复合体;抑制解除-痴呆-帕金森神经机能障碍-肌肉萎缩复合体;抑制解除-痴呆-帕金森神经机能障碍-肌萎缩复合体;抑制解除-痴呆-帕金森综合征-肌萎缩复合体;抑制解除-痴呆-震颤性麻痹-肌肉萎缩复合体;抑制解除-痴 全血或组织;血液/组织;血液或组织 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 分类型应答;分类型结果;名义性;名称型;名词型;名词性;标称性;没有自然次序的名义型或分类型应答 基因突变分析 存在;存在与否;特征标识;身份;身份标识 时刻;随机;随意;瞬间 未作说明的组织;组织;组织 & 涂片 血;血液 遗传基因;遗传因子;吉恩;生物基因

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