174 Genes
| Gene | Ensembl | Entrez | Aliases | Map Position | SwissProt ID | SwissProt Description | Subcellular Locations | Subcell PMIDs | Protein Complex | OMIM Gene | OMIM Disease |
|---|---|---|---|---|---|---|---|---|---|---|---|
| UCP3 | ENSG00000175564 | 7352 | SLC25A9 | 11q13 | P55916 | Mitochondrial uncoupling protein 3 | Mitochondria Mitochondrial-inner-membrane | 10631320 | Uncoupling protein complex (UCP) | 602044 | Noninsulin dependent diabetes mellitus (NIDDM) [125853]; Obesity [601665] |
| UNG | ENSG00000076248 | 7374 | DGU; DKFZp781L1143; HIGM4; UDG; UNG1; UNG15 | 12q23-q24.1 | P13051 | Uracil-DNA glycosylase (UDG) | Mitochondria Nucleus | 12958596 | 191525 | Immunodeficiency with hyper IgM type 5 (HIGM5) [608106] | |
| UQCRB | ENSG00000156467 | 7381 | QP-C; QPC; UQBC; UQBP; UQPC | 8q22 | P14927 | Ubiquinol-cytochrome c reductase complex 14 kDa protein | Mitochondria Mitochondrial-inner-membrane | 12709789 | Respiratory chain complex III (RCCIII) | 191330 | Deficiency of respiratory chain complex III (RCC3) [124000] |
| UROS | ENSG00000188690 | 7390 | - | 10q25.2-q26.3 | P10746 | Uroporphyrinogen-III synthase | Cytoplasm Mitochondria-related | 3792391 7597845 | 606938 | Congenital erythropoietic porphyria (CEP) [263700] | |
| WFS1 | ENSG00000109501 | 7466 | DFNA14; DFNA38; DFNA6; DIDMOAD; WFRS; WFS; WOLFRAMIN | 4p16 | O76024 | Wolframin | Endoplasmatic-reticulum Mitochondria-related | 9771706 9817917 16195229 | 606201 | Wolfram syndrome (DIDMOAD) [222300]; Autosomal dominant nonsyndromic sensorineural deafness (DFNA6) [600965] | |
| WWOX | ENSG00000186153 | 51741 | D16S432E; FOR; FRA16D; HHCMA56; PRO0128; WOX1; WWOX v8 | 16q23.3-q24.1 | Q9NZC7 | Oxidoreductase | Cytoplasm Mitochondria Nucleus | 10786676 11744990 14695174 15664696 | 605131 | Esophageal squamous cell carcinoma (ESCC) [133239]; Pancreatic carcinoma [260350] |
