| ID: 7067 | thyroid hormone receptor alpha [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (40062193..40093867) | AR7, CHNG6, EAR7, ERB-T-1, ERBA, ERBA1, NR1A11, THRA2, THRalpha, THRalpha1, THRalpha2, TRalpha, TRalpha1, TRalpha2, c-ERBA-1, c-erbA, THRA | 190120 |
| ID: 51177 | pleckstrin homology domain containing O1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (150149646..150160065) | CKIP-1, CKIP1, JBP, OC120 | 608335 |
| ID: 5100 | protocadherin 8 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (52842889..52848640, complement) | ARCADLIN, PAPC | 603580 |
| ID: 2572 | glutamate decarboxylase 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (26216372..26304558) | GAD65 | 138275 |
| ID: 10817 | fibroblast growth factor receptor substrate 3 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (41770176..41779900, complement) | FRS2-beta, FRS2B, FRS2beta, SNT-2, SNT2 | 607744 |
| ID: 56896 | dihydropyrimidinase like 5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (26847995..26950351) | CRAM, CRMP-5, CRMP5, CV2, RTSC4, Ulip6 | 608383 |
| ID: 57348 | tweety family member 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (54415464..54436904) | | 605784 |
| ID: 140679 | solute carrier family 32 member 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38724486..38729372) | DEE114, GEFSP12, VGAT, VIAAT, VIAAT GEFSP12 | 616440 |
| ID: 56243 | KIAA1217 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (23694727..24547843) | ETL4, SKT | 617367 |
| ID: 79683 | zinc finger DHHC-type palmitoyltransferase 14 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (157381190..157678157) | NEW1CP | 619295 |
| ID: 478 | ATPase Na+/K+ transporting subunit alpha 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (41966582..41994230, complement) | AHC2, ATP1A1, CAPOS, DEE99, DYT12, RDP | 182350 |
| ID: 23193 | glucosidase II alpha subunit [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (62624829..62646613, complement) | G2AN, GIIA, GIIalpha, GLUII, PKD3 | 104160 |
| ID: 30010 | neurexophilin 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (8433609..8752961) | NPH1, Nbla00697 | 604639 |
| ID: 85395 | SLX9 ribosome biogenesis factor [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44939697..44976973) | C21orf70, FAM207A, PRED56 | |
| ID: 57338 | junctophilin 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87601835..87698156) | CAGL237, HDL2, JP-3, JP3, TNRC22 | 605268 |
| ID: 5465 | peroxisome proliferator activated receptor alpha [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (46150526..46243756) | NR1C1, PPAR, PPAR-alpha, PPARalpha, hPPAR | 170998 |
| ID: 55343 | solute carrier family 35 member C1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (45804079..45813016) | CDG2C, FUCT1 | 605881 |
| ID: 4062 | lymphocyte antigen 6 family member H [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143157916..143160654, complement) | NMLY6 | 603625 |
| ID: 375323 | LHFPL tetraspan subfamily member 4 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (9498361..9553822, complement) | GARLH4 | 610240 |
| ID: 220107 | deleted in lymphocytic leukemia 7 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50711026..50843939, complement) | | 618634 |