| ID: 90639 | cytochrome c oxidase assembly factor COX19 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (964852..975549, complement) | | 610429 |
| ID: 9131 | apoptosis inducing factor mitochondria associated 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (130129362..130165841, complement) | AIF, AUNX1, CMT2D, CMTX4, COWCK, COXPD6, DFNX5, NADMR, NAMSD, PDCD8, SEMDHL | 300169 |
| ID: 538 | ATPase copper transporting alpha [Homo sapiens (human)] | Chromosome X, NC_000023.11 (77910693..78050395) | DSMAX, HMNX, MK, MNK, SMAX3 | 300011 |
| ID: 1445 | C-terminal Src kinase [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (74782080..74803197) | | 124095 |
| ID: 346389 | MET transcriptional regulator MACC1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (20134655..20217384, complement) | 7A5, SH3BP4L | 612646 |
| ID: 94081 | sideroflexin 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (175478560..175529742) | SLC56A1, TCC | 615569 |
| ID: 55486 | presenilin associated rhomboid like [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (183826489..183884880, complement) | PRO2207, PSARL, PSARL1, PSENIP2, RHBDS1 | 607858 |
| ID: 6341 | synthesis of cytochrome C oxidase 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (10672474..10697533, complement) | MC4DN4, SCOD1 | 603644 |
| ID: 11033 | ArfGAP with dual PH domains 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (897900..955407, complement) | CENTA1, GCS1L, p42IP4 | 608114 |
| ID: 54764 | zinc finger RANBP2-type containing 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (124916894..124988189) | TRABID | 611749 |
| ID: 1353 | cytochrome c oxidase copper chaperone COX11 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (54951902..54968785, complement) | COX11P, MC4DN23 | 603648 |
| ID: 57017 | coenzyme Q9 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (57447479..57461270) | C16orf49, COQ10D5 | 612837 |