53847-0
CACT gene targeted mutation analysis in Blood or Tissue by Molecular genetics method
Active
Part Description
LP71411-0 CACT gene
The CACT gene (solute carrier family 25 (carnitine/acylcarnitine translocase), member 20) gene is located on chromosome 3p21.31. This gene product is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. This protein mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants. [provided by RefSeq, Jul 2008] [NCBI Gene ID:788]
Source: National Center for Biotechnology Information (NCBI) Gene
LOINC Names Get Info
- Fully-Specified Name
- CACT gene targeted mutation analysis:
Find: Pt: Bld/Tiss: Doc: Molgen - Long Common Name
- CACT gene targeted mutation analysis in Blood or Tissue by Molecular genetics method
- Short Name
- CACT gene Mut Anl Bld/T
- Display Name
- CACT gene targeted mutation analysis Molgen Doc (Bld/Tiss)
- Consumer Name Alpha Get Info
- CACT gene targeted mutation analysis, Blood or tissue specimen
Part Model Get Info
- Component
- CACT gene targeted mutation analysis
LP227860-6
- Analyte
- CACT gene targeted mutation analysis
LP227860-6
- Component Numerator
- CACT gene targeted mutation analysis
LP227860-6
- 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.MUT
- Type
- Laboratory
- First Released
- Version 2.26
- Last Updated
- Version 2.68 (MIN)
- 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
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| cs-CZ | Czech (Czechia) | Gen CACT cílená mutační analýza: |
| el-GR | Greek (Greece) | Γονίδιο CACT στοχευμένη ανάλυση μεταλλάξεων: Synonyms: Doc MOLPATH MOLPATH.MUT Pt Αίμα Αίμα/Ιστός Γονίδιο Γονίδιο CACT Εύρεση Ιστός Μοριακή γενετική στοχευμένη ανάλυση μεταλλάξεων |
| es-ES | Spanish (Spain) | Gen CACT Analisis de mutaciones: |
| es-MX | Spanish (Mexico) | Análisis de mutaciones dirigidas al gen CACT: |
| fr-FR | French (France) | CACT gène mutation cible trouvée: |
| it-IT | Italian (Italy) | CACT, gene analisi di mutazione mirata: Synonyms: Gene CACT Genetica molecolare Mutazione genica Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & |
| nl-NL | Dutch (Netherlands) | CACT-gen doelgerichte mutatie-analyse: Synonyms: CACT gen molgen targeted |
| pl-PL | Polish (Poland) | CACT gen ukierunkowana analiza mutacji: Synonyms: Analiza mutacji genu CACT diagnostyka molekularna Gen CACT |
| pt-BR | Portuguese (Brazil) | CACT análise de mutação genética: Synonyms: Identity or presence; |
| ru-RU | Russian (Russian Federation) | CACT ген исследование на мутацию: Synonyms: Документ Кровь Кровь или Ткань Ткань и мазки Точка во времени; |
| tr-TR | Turkish (Turkey) | CACT geni Mutasyon analizi: |
| zh-CN | Chinese (China) | CACT 基因 突变分析: Synonyms: 临床文档型; |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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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://