Gene table of FOXRED1 : FAD dependent oxidoreductase domain containing 1

Gene-disease associations table

Disease IDDisease nameSource of annotation with FOXRED1OMIM linkNumber of associated genesgenes
252010MITOCHONDRIAL COMPLEX I DEFICIENCYOMIM, HUMSAVAR link to OMIM 24MT-ND5, NDUFAF2, MT-ND6, NDUFS2, NDUFAF6, NDUFAF1, NDUFAF5, NDUFV1, NUBPL, NDUFS7, MT-ND1, NDUFS3, NDUFA1, NDUFS6, NDUFV2, NDUFAF4, MT-ND3, NDUFAF3, NDUFS1, NDUFB9, NDUFA11, NDUFS4, NDUFB3, FOXRED1
256000LEIGH SYNDROMEOMIM link to OMIM 27MT-ND5, NDUFAF2, NDUFA12, NDUFAF6, NDUFV1, NDUFA10, MTFMT, NDUFS8, BCS1L, SDHA, MT-CO3, COX10, NDUFA2, ECHS1, NDUFS3, MT-ATP6, SURF1, MT-ND3, IARS2, NARS2, NDUFS7, COX15, NDUFAF5, POLG, FOXRED1, NDUFS4, NDUFA9

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Annotation of the gene FOXRED1

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
catalytic activityGO:00038241.05
oxidoreductase activityGO:00164913.12