| ID: 23133 | PHD finger protein 8 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (53936680..54048936, complement) | JHDM1F, KDM7B, MRXSSD, ZNF422 | 300560 |
| ID: 6991 | dynein light chain Tctex-type 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (169725091..169751572, complement) | TCTE3, TCTEX1D3, TCTEX2, Tctex4, oda12 | 186977 |
| ID: 23154 | neurochondrin [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (35557799..35566779) | NEDIES | 608458 |
| ID: 80028 | F-box and leucine rich repeat protein 18 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (5454425..5513809, complement) | Fbl18 | 609084 |
| ID: 644096 | succinate dehydrogenase complex assembly factor 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (35995188..35996312) | LYRM8, MC2DN2 | 612848 |
| ID: 221785 | zinc finger and SCAN domain containing 25 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (99616946..99738035) | ZNF498 | |
| ID: 23161 | sorting nexin 13 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (17790761..17940494, complement) | RGS-PX1 | 606589 |
| ID: 56913 | core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (7157377..7248616) | C1GALT, T-synthase | 610555 |
| ID: 22803 | 5'-3' exoribonuclease 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (21303331..21389825) | | 608851 |
| ID: 6618 | small nuclear RNA activating complex polypeptide 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (7920338..7923250) | PTFDELTA, SNAP45 | 605076 |
| ID: 55249 | YY1 associated protein 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155659442..155688996, complement) | GRNG, HCCA1, HCCA2, YY1AP | 607860 |
| ID: 7818 | death associated protein 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155687948..155739010) | DAP-3, MRP-S29, MRPS29, S29mt, bMRP-10, mS29 | 602074 |
| ID: 10962 | MLLT11 transcription factor 7 cofactor [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151060397..151069544) | AF1Q | 604684 |
| ID: 55780 | ER membrane associated RNA degradation [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (169751306..169781600) | C6orf70, PVNH6, dJ266L20.3 | 615532 |
| ID: 56882 | CDC42 small effector 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151050985..151059622, complement) | SCIP1, SPEC1 | 619456 |
| ID: 8209 | glutamine amidotransferase class 1 domain containing 3 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44133683..44145711) | C21orf33, ES1A, GT335, HES1, KNPH, KNPI, GATD3 | 601659 |
| ID: 1845 | dual specificity phosphatase 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43766125..43778977, complement) | VHR | 600183 |
| ID: 9159 | proprotein convertase subtilisin/kexin type 7 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (117204337..117232073, complement) | LPC, PC7, PC8, SPC7 | 604872 |
| ID: 257415 | family with sequence similarity 133 member B [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (92560758..92590390, complement) | | |
| ID: 83475 | deoxyhypusine hydroxylase [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3490824..3500674, complement) | HLRC1, NEDMVIC, hDOHH | 611262 |