| ID: 5959 | retinol dehydrogenase 5 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (55720393..55724705) | 9cRDH, HSD17B9, RDH1, SDR9C5 | 601617 |
| ID: 100528022 | BLOC1S1-RDH5 readthrough [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (55716034..55724742) | | |
| ID: 1994 | ELAV like RNA binding protein 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (7958573..8005641, complement) | ELAV1, HUR, Hua, MelG | 603466 |
| ID: 4286 | melanocyte inducing transcription factor [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (69739464..69968332) | CMM8, COMMAD, MI-A, WS2, WS2A, bHLHe32, MITF | 156845 |
| ID: 6017 | retinaldehyde binding protein 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (89209869..89221579, complement) | CRALBP | 180090 |
| ID: 5000 | origin recognition complex subunit 4 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (147930396..148021551, complement) | ORC4LP, ORC4 | 603056 |
| ID: 7326 | ubiquitin conjugating enzyme E2 G1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (4269259..4366675, complement) | E217K, UBC7, UBE2G | 601569 |
| ID: 5995 | retinal G protein coupled receptor [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (84245053..84259960) | RP44 | 600342 |
| ID: 2647 | biogenesis of lysosomal organelles complex 1 subunit 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (55716046..55719703) | BLOS1, BORCS1, GCN5L1, MICoA, RT14 | 601444 |
| ID: 64841 | glucosamine-phosphate N-acetyltransferase 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (52775193..52791607, complement) | GNA1, GNPNAT, Gpnat1, RHZDAN | 616510 |
| ID: 8916 | HECT and RLD domain containing E3 ubiquitin protein ligase 3 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (88523843..88708539) | | 605200 |
| ID: 84301 | DNA damage inducible 1 homolog 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (15617458..15669044) | | |
| ID: 283458 | NME2 pseudogene 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (120282218..120282856) | | |