Entity Details

Primary name SLC25A26
Entity type gene
Source Source Link

Details

PrimaryID115286
RefseqGeneNG_054637
SymbolSLC25A26
Namesolute carrier family 25 member 26
Chromosome3
Location3p14.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-10-04
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsSAMC_HUMAN

GO terms

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GOName
GO:0000095 S-adenosyl-L-methionine transmembrane transporter activity
GO:0005739 mitochondrion
GO:0005743 mitochondrial inner membrane
GO:0006811 ion transport
GO:0015805 S-adenosyl-L-methionine transport
GO:0016021 integral component of membrane

Diseases

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Disease IDSourceNameDescription
616794 OMIMCombined oxidative phosphorylation deficiency 28 (COXPD28)An autosomal recessive mitochondrial disorder characterized by decreased activities of respiratory chain enzymes, and variable clinical manifestations. Clinical features include episodic metabolic decompensation beginning in infancy, mild muscle weakness, cardiorespiratory insufficiency, developmental delay, or even death. The disease is caused by variants affecting the gene represented in this entry.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
SLC25A26FBXO7BioGRID27503909 details
SLC25A26MARCHF5BioGRID26813789 details
SLC25A26SPACA1BioGRID, IntAct26186194 28514442 details
SLC25A26DUSP23BioGRID27432908 details