Gene table of SLC25A20 : solute carrier family 25 member 20

Gene-disease associations table

Disease IDDisease nameSource of annotation with SLC25A20OMIM linkNumber of associated genesgenes
212138CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCYClinVar, OMIM, HUMSAVAR link to OMIM 1SLC25A20

Download the gene annotation in CSV format

Annotation of the gene SLC25A20

Associated genes in ENSEMBL
Associated proteins - SwissProt Accession ID
Associated PDB IDs
Cytogenetic Band
Tandem repeats annotation
Transcription regulation as annotated in TRRUST

It is regulated by the following TF:

Associated KEGG pathways
Associated REACTOME pathways
REACTOME pathwayREACTOME IDREACTOME IC
Metabolism of lipids and lipoproteinsR-HSA-5568333.79
Import of palmitoyl-CoA into the mitochondrial matrixR-HSA-2004259.52
MetabolismR-HSA-14307282.34
Fatty acid, triacylglycerol, and ketone body metabolismR-HSA-5357345.44
Associated GO terms for Molecular function
GO termGO IDGO IC
substrate-specific transmembrane transporter activityGO:00228912.9
structural constituent of ribosomeGO:00037354.32
substrate-specific transporter activityGO:00228922.72
quaternary ammonium group transmembrane transporter activityGO:00156517.66
acyl carnitine transmembrane transporter activityGO:00152279.05
transporter activityGO:00052152.57
cation transmembrane transporter activityGO:00083243.32
structural molecule activityGO:00051983.1
ion transmembrane transporter activityGO:00150753.04
transmembrane transporter activityGO:00228572.82
organic cation transmembrane transporter activityGO:00151017.34