| ID: 51167 | cytochrome b5 reductase 4 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (83859689..83967423) | NCB5OR, cb5/cb5R, dJ676J13.1 | 608343 |
| ID: 79736 | transcription elongation factor, mitochondrial [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30898986..30906238, complement) | C17orf42, COXPD58 | 616422 |
| ID: 10793 | zinc finger protein 273 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (64877603..64937316) | HZF9 | 604756 |
| ID: 6871 | transcriptional adaptor 2A [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37406886..37479725) | ADA2, ADA2A, KL04P, TADA2L, hADA2 | 602276 |
| ID: 5886 | RAD23 homolog A, nucleotide excision repair protein [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12945862..12953642) | HHR23A, HR23A | 600061 |
| ID: 8615 | USO1 vesicle transport factor [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (75724577..75814286) | P115, TAP, VDP | 603344 |
| ID: 2618 | phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (33503931..33542893, complement) | AIRS, GARSF, PAIS, PGFT, PRGS, GART | 138440 |
| ID: 10440 | translocase of inner mitochondrial membrane 17A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201955503..201970664) | TIM17, TIM17A | 605057 |
| ID: 54952 | tRNA selenocysteine 1 associated protein 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (28553085..28578545) | PRO1902, SECP43, TRSPAP1 | 619597 |
| ID: 10856 | RuvB like AAA ATPase 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (48993448..49015995) | CGI-46, ECP-51, ECP51, INO80J, REPTIN, RVB2, TAP54-beta, TIH2, TIP48, TIP49B | 604788 |
| ID: 84313 | vacuolar protein sorting 25 homolog [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42773449..42779599) | DERP9, EAP20, FAP20 | 610907 |
| ID: 51427 | zinc finger protein 107 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (64666133..64711577) | Y8, ZFD25, ZNF588, smap-7 | 603989 |
| ID: 63929 | X-prolyl aminopeptidase 3 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (40857148..40932815) | APP3, ICP55, NPHPL1 | 613553 |
| ID: 84259 | defective in cullin neddylation 1 domain containing 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (103050686..103092160, complement) | DCNL5, SCCRO5 | 616522 |
| ID: 80345 | zinc finger and SCAN domain containing 16 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (28124609..28130082) | ZNF392, ZNF435, dJ265C24.3 | 618544 |
| ID: 54521 | WD repeat domain 44 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (118346073..118449961) | RAB11BP, RPH11, SYM-4 | 301070 |
| ID: 285636 | RAB7A interacting MON1-CCZ1 complex subunit 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (41904344..41921636) | C5orf51 | 620266 |