Gene table of SLC25A15 : solute carrier family 25 member 15

Gene-disease associations table

Disease IDDisease nameSource of annotation with SLC25A15OMIM linkNumber of associated genesgenes
238970HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROMEClinVar, OMIM, HUMSAVAR link to OMIM 1SLC25A15

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Annotation of the gene SLC25A15

Associated genes in ENSEMBL
Associated proteins - SwissProt Accession ID
Associated PDB IDs
Cytogenetic Band
Tandem repeats annotation
Transcription regulation as annotated in TRRUST
Associated KEGG pathways
Associated REACTOME pathways
REACTOME pathwayREACTOME IDREACTOME IC
Urea cycleR-HSA-706359.81
Metabolism of amino acids and derivativesR-HSA-712915.4
MetabolismR-HSA-14307282.34
Associated GO terms for Molecular function
GO termGO IDGO IC
substrate-specific transmembrane transporter activityGO:00228912.9
substrate-specific transporter activityGO:00228922.72
organic acid transmembrane transporter activityGO:00053424.97
L-ornithine transmembrane transporter activityGO:00000648.13
transporter activityGO:00052152.57
structural molecule activityGO:00051983.1
structural constituent of ribosomeGO:00037354.32
transmembrane transporter activityGO:00228572.82
L-amino acid transmembrane transporter activityGO:00151796.0
amino acid transmembrane transporter activityGO:00151715.38
carboxylic acid transmembrane transporter activityGO:00469434.99