48600-1
VPS13B gene targeted mutation analysis in Blood or Tissue by Molecular genetics method
Active
Part Description
LP62804-7 VPS13B gene
The VPS13B gene (vacuolar protein sorting 13 homolog B (yeast)) [HGNC Gene ID:2183] is located on chromosome 8q22.2. This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008] [NCBI Gene ID:157680]
Source: National Center for Biotechnology Information (NCBI) Gene
LOINC Names Get Info
- Fully-Specified Name
- VPS13B gene targeted mutation analysis:
Find: Pt: Bld/Tiss: Doc: Molgen - Long Common Name
- VPS13B gene targeted mutation analysis in Blood or Tissue by Molecular genetics method
- Short Name
- VPS13B gene Mut Anl Bld/T
- Display Name
- VPS13B gene targeted mutation analysis Molgen Doc (Bld/Tiss)
- Consumer Name Alpha Get Info
- VPS13B gene targeted mutation analysis, Blood or tissue specimen
Part Model Get Info
- Component
- VPS13B gene targeted mutation analysis
LP229930-5
- Analyte
- VPS13B gene targeted mutation analysis
LP229930-5
- Component Numerator
- VPS13B gene targeted mutation analysis
LP229930-5
- 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 2.21
- Last Updated
- Version 2.73 (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
- Common Test Rank Get Info
- 7723
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| cs-CZ | Czech (Czechia) | Gen VPS13B cílená mutační analýza: |
| el-GR | Greek (Greece) | Γονίδιο VPS13B στοχευμένη ανάλυση μεταλλάξεων: Synonyms: Doc MOLPATH MOLPATH.MUT Pt Αίμα Αίμα/Ιστός Γονίδιο Γονίδιο VPS13B Εύρεση Ιστός Μοριακή γενετική στοχευμένη ανάλυση μεταλλάξεων |
| es-ES | Spanish (Spain) | Gen VPS13B Analisis de mutaciones: |
| es-MX | Spanish (Mexico) | Análisis de mutaciones dirigidas al gen VPS13B: |
| fr-FR | French (France) | VPS13B gène mutation cible trouvée: |
| it-IT | Italian (Italy) | VPS13B, gene analisi di mutazione mirata: Synonyms: Gene VPS13B Genetica molecolare Mutazione genica Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & |
| nl-NL | Dutch (Netherlands) | VPS13B-gen doelgerichte mutatie-analyse: Synonyms: molgen targeted VPS13B gen |
| pl-PL | Polish (Poland) | VPS13B gen ukierunkowana analiza mutacji: Synonyms: Analiza mutacji genu VPS13B diagnostyka molekularna Gen VPS13B |
| pt-BR | Portuguese (Brazil) | VPS13B análise de mutação genética: Synonyms: CHS1; |
| ru-RU | Russian (Russian Federation) | VPS13B ген исследование на мутацию: Synonyms: Документ Кровь Кровь или Ткань Ткань и мазки Точка во времени; |
| tr-TR | Turkish (Turkey) | VPS13B geni Mutasyon analizi: |
| zh-CN | Chinese (China) | VPS13B 基因 突变分析: Synonyms: CHS1; |
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://