| ID: 149986 | LSM family member 14B [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (62122475..62135374) | C20orf40, FAM61B, FT005, LSM13, RAP55B, bA11M20.3 | 620689 |
| ID: 10743 | retinoic acid induced 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (17681458..17811453) | SMCR, SMS | 607642 |
| ID: 130507 | ubiquitin protein ligase E3 component n-recognin 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (169827454..170084131) | ZNF650 | 613831 |
| 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: 23446 | solute carrier family 44 member 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (105244651..105438504) | CD92, CDW92, CHTL1, CONATOC, CTL1 | 606105 |
| ID: 23030 | lysine demethylase 4B [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (4969113..5153598) | JMJD2B, MRD65, TDRD14B | 609765 |
| ID: 55690 | phosphofurin acidic cluster sorting protein 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66070272..66244744) | MRD17, SHMS | 607492 |
| ID: 23181 | disco interacting protein 2 homolog A [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46458891..46583871) | C21orf106, DIP2 | 607711 |
| ID: 6418 | SET nuclear proto-oncogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128683424..128696396) | 2PP2A, I2PP2A, IGAAD, IPP2A2, MRD58, PHAPII, TAF-I, TAF-IBETA | 600960 |
| ID: 3267 | ArfGAP with FG repeats 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227472156..227561217) | HRB, RAB, RIP | 600862 |
| ID: 317781 | DEAD-box helicase 51 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (132136594..132144319, complement) | | |
| ID: 10498 | coactivator associated arginine methyltransferase 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10871553..10923075) | PRMT4 | 603934 |
| ID: 9444 | QKI, KH domain containing RNA binding [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (163414718..163578592) | Hqk, QK, QK1, QK3, hqkI | 609590 |
| ID: 11275 | kelch like family member 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (165207561..165323156) | ABP-KELCH, MAV, MAYVEN | 605774 |
| ID: 2771 | G protein subunit alpha i2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (50227068..50263358) | GIPB, HG1C, H_LUCA15.1, H_LUCA16.1, GNAI2 | 139360 |
| ID: 2782 | G protein subunit beta 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (1785286..1891087, complement) | HG2A, MDS, MRD42 | 139380 |
| ID: 93624 | transcriptional adaptor 2B [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (7043372..7057952) | ADA2(beta), ADA2B | 608790 |
| ID: 51542 | VPS54 subunit of GARP complex [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (63892150..64019428, complement) | HCC8, PPP1R164, SLP-8pL, WR, hVps54L, VPS54 | 614633 |
| ID: 3297 | heat shock transcription factor 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144291604..144314720) | HSTF1 | 140580 |
| ID: 23095 | kinesin family member 1B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10210570..10381603) | CMT2, CMT2A, CMT2A1, HMSNII, KLP, NBLST1 | 605995 |