Gene table of SLC25A26 : solute carrier family 25 member 26

Gene-disease associations table

Disease IDDisease nameSource of annotation with SLC25A26OMIM linkNumber of associated genesgenes
PS609060COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCYClinVar, OMIM link to OMIM 29C12orf65, FARS2, GFM1, TARS2, MTFMT, MTO1, AIFM1, EARS2, NARS2, SFXN4, MRPS22, PNPT1, TSFM, ATP5A1, LYRM4, SLC25A26, MRPS16, MRPL3, TUFM, TRMT5, MRPL44, GTPBP3, VARS2, CARS2, RMND1, ELAC2, AARS2, TXN2, MARS2

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Annotation of the gene SLC25A26

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
Associated GO terms for Molecular function
GO termGO IDGO IC
coenzyme transporter activityGO:00511858.13
cofactor transporter activityGO:00511846.69
sulfur compound transmembrane transporter activityGO:19016826.44
S-adenosyl-L-methionine transmembrane transporter activityGO:00000959.74
transporter activityGO:00052152.57
modified amino acid transmembrane transporter activityGO:00723496.97
structural molecule activityGO:00051983.1
structural constituent of ribosomeGO:00037354.32
transmembrane transporter activityGO:00228572.82