94217-7
TP53 gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method
Active
Term Description
Test includes full sequence analysis and deletion/duplication analysis for the detection of variants and large deletions/duplications in the TP53 gene. Testing may be performed to identify mutations associated with a variety of human cancers, including hereditary cancers such as Li-Fraumeni syndrome.[GHR gene: TP53]
Part Description
LP19769-6 TP53 gene
The TP53 gene (tumor protein p53) [HGNC Gene ID:11998] is located on chromosome 17p13.1. This gene encodes a tumor suppressor protein containing transcriptional activation, DNA binding, and oligomerization domains. The encoded protein responds to diverse cellular stresses to regulate expression of target genes, thereby inducing cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. Mutations in this gene are associated with a variety of human cancers, including hereditary cancers such as Li-Fraumeni syndrome. Alternative splicing of this gene and the use of alternate promoters result in multiple transcript variants and isoforms. Additional isoforms have also been shown to result from the use of alternate translation initiation codons (PMIDs: 12032546, 20937277). [provided by RefSeq, Feb 2013] [NCBI Gene ID:7157]
Source: National Center for Biotechnology Information (NCBI) Gene
LOINC Names Get Info
- Fully-Specified Name
- TP53 gene deletion+duplication & full mutation analysis:
Find: Pt: Bld/Tiss: Doc: Molgen - Long Common Name
- TP53 gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method
- Short Name
- TP53 gene Del+Dup + Full Mut Anl Bld/T
- Display Name
- TP53 gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)
- Consumer Name Alpha Get Info
- TP53 gene variant analysis, Blood or tissue specimen
Part Model Get Info
- Component
- TP53 gene deletion+duplication & full mutation analysis
LP417514-9
- Analyte
- TP53 gene deletion+duplication & full mutation analysis
LP417514-9
- Component Numerator
- TP53 gene deletion+duplication & full mutation analysis
LP417514-9
- Component Numerator Core
- TP53 gene
LP19769-6
- Component Numerator Core Suffix
- deletion+duplication & full mutation analysis
LP200206-3
- Component Denominator
- NULL
- Component Denominator Core
- NULL
- Component Denominator Core Suffix
- NULL
- Challenge
- NULL
- Adjustment
- NULL
- Count
- NULL
- Property
- Find
LP6813-2
- Time
- Pt
LP6960-1
- Time Core
- Pt
LP6960-1
- Time Modifier
- NULL
- System
- Bld/Tiss
LP7061-7
- System Core
- Bld/Tiss
LP7061-7
- Super System
- NULL
- Scale
- Doc
LP32888-7
- Method
- Molgen
LP6404-0
Basic Attributes
- Class
- MOLPATH
- Type
- Laboratory
- First Released
- Version 2.68
- Last Updated
- Version 2.68 (ADD)
- Order vs. Observation
- Both
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| cs-CZ | Czech (Czechia) | Gen TP53 delece+duplikace a kompletní mutační analýza: |
| el-GR | Greek (Greece) | Γονίδιο TP53 ανάλυση διαγραφής+διπλασιασμού & πλήρους μετάλλαξης: Synonyms: Doc MOLPATH Pt Αίμα Αίμα/Ιστός ανάλυση διαγραφής+διπλασιασμού & |
| es-ES | Spanish (Spain) | Gen TP53 estudio delecion+duplicacion y estudio mutacional completo: |
| es-MX | Spanish (Mexico) | Eliminación del gen TP53 + análisis de duplicación y mutación completa: |
| fr-FR | French (France) | TP53 gène délétion+duplication et analyse complète des mutations: |
| it-IT | Italian (Italy) | TP53, gene Delezione+duplicazione & analisi di mutazione completa: Synonyms: delezione e duplicazione Gene Tp53 Genetica molecolare Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & |
| nl-NL | Dutch (Netherlands) | TP53-gen deletie + duplicatie & volledige mutatie analyse: Synonyms: molgen TP53 gen |
| pl-PL | Polish (Poland) | TP53 gen delecja+duplikacja i pełna analiza mutacji: Synonyms: diagnostyka molekularna Gen TP53 |
| tr-TR | Turkish (Turkey) | TP53 geni delesyon+duplikasyon ve tam mutasyon analizi: Synonyms: çiftleme |
| zh-CN | Chinese (China) | TP53 基因 缺失+重复与全面的突变分析: Synonyms: Li-Fraumeni 综合征; |
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LOINC Copyright
Copyright © Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://