Description

The SLC25A20 gene (solute carrier family 25 member 20) [HGNC Gene ID:1421] 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

Basic Part Properties

Part Name
SLC25A20 gene
Part Display Name
SLC25A20 gene
Part Type
Component (Describes the core component or analyte measured)
Created On
2020-01-13
Construct for LOINC Short Name
SLC25A20

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Language Variants Get Info

TagLanguageTranslation
nl-NLDutch (Netherlands)SLC25A20-gen
zh-CNChinese (China)SLC25A20 基因
Synonyms: 溶质载体家族 25 成员 20 基因;Solute Carrier Family 25 Member 20 gene
fr-FRFrench (France)SLC25A20 gène
it-ITItalian (Italy)SLC25A20, gene
es-ESSpanish (Spain)Gen SLC25A20
pl-PLPolish (Poland)SLC25A20 gen
Synonyms: Gen SLC25A20
el-GRGreek (Greece)Γονίδιο SLC25A20
Synonyms: Γονίδιο SLC25A20