LP208423-6
SLC26A2 gene
Active
Description
The SLC26A2 gene (solute carrier family 26 member 2) [HGNC Gene ID:10994] is located on chromosome 5q32. The diastrophic dysplasia sulfate transporter is a transmembrane glycoprotein implicated in the pathogenesis of several human chondrodysplasias. It apparently is critical in cartilage for sulfation of proteoglycans and matrix organization. [provided by RefSeq, Jul 2008] [NCBI Gene ID:1836] Source: National Center for Biotechnology Information (NCBI) Gene
Basic Part Properties
- Part Name
- SLC26A2 gene
- Part Display Name
- SLC26A2 gene
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2016-03-17
- Construct for LOINC Short Name
- SLC26A2
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| zh-CN | Chinese (China) | SLC26A2 基因 Synonyms: 溶质载体家族 26 成员 2; |
| es-ES | Spanish (Spain) | Gen SLC26A2 |
| it-IT | Italian (Italy) | SLC26A2, gene Synonyms: Gene SLC26A2 |
| nl-NL | Dutch (Netherlands) | SLC26A2-gen Synonyms: SLC26A2 gen |
| fr-FR | French (France) | SLC26A2 gène |
| pl-PL | Polish (Poland) | SLC26A2 gen Synonyms: Gen SLC26A2 |
| el-GR | Greek (Greece) | Γονίδιο SLC26A2 Synonyms: Γονίδιο SLC26A2 |
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://