ID: 8604 | solute carrier family 25 member 12 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171783405..171894244, complement) | AGC1, ARALAR, DEE39, EIEE39 | 603667 |
ID: 84661 | dpy-30 histone methyltransferase complex regulatory subunit [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (32011649..32039835, complement) | Cps25, HDPY-30, Saf19 | 612032 |
ID: 6170 | ribosomal protein L39 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (119786504..119791630, complement) | L39P42, RPL39_23_1806, eL39, RPL39 | 300899 |
ID: 51141 | insulin induced gene 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118088471..118110997) | INSIG-2 | 608660 |
ID: 54969 | histone PARylation factor 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169729470..169757944, complement) | C4orf27 | 616614 |
ID: 80304 | WD repeat and coiled coil containing [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (24029347..24047391, complement) | C2orf44, MMAP, PP384 | 616234 |
ID: 374291 | NADH:ubiquinone oxidoreductase core subunit S7 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (1383907..1395584) | CI-20, CI-20KD, MC1DN3, MY017, PSST | 601825 |
ID: 2956 | mutS homolog 6 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (47783145..47810101) | GTBP, GTMBP, HNPCC5, HSAP, LYNCH5, MMRCS3, MSH-6, p160 | 600678 |
ID: 26043 | UBX domain protein 7 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196347662..196432427, complement) | UBXD7 | 616379 |
ID: 9262 | serine/threonine kinase 17b [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (196133583..196176483, complement) | DRAK2 | 604727 |
ID: 65062 | transmembrane protein 237 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (201620186..201643503, complement) | ALS2CR4, JBTS14 | 614423 |
ID: 55746 | nucleoporin 133 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (229440259..229508341, complement) | GAMOS8, NPHS18, hNUP133 | 607613 |
ID: 55248 | proton activated chloride channel 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212363928..212414886, complement) | ASOR, C1orf75, PAC, PAORAC, TMEM206, hPAC, hTMEM206 | 618427 |
ID: 11127 | kinesin family member 3A [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (132688812..132737546, complement) | FLA10, KLP-20 | 604683 |
ID: 2272 | fragile histidine triad diadenosine triphosphatase [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (59747277..61251452, complement) | AP3Aase, FRA3B | 601153 |
ID: 84984 | centrosomal protein 19 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196706277..196712250, complement) | C3orf34, MOSPGF | 615586 |
ID: 2177 | FA complementation group D2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (10026437..10101932) | FA-D2, FA4, FACD, FAD, FAD2, FANCD | 613984 |
ID: 79862 | zinc finger protein 669 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (247099962..247104356, complement) | | |
ID: 201931 | transmembrane protein 192 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (165070608..165112860, complement) | | 620677 |
ID: 23178 | PAS domain containing serine/threonine kinase [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241106099..241150347, complement) | PASKIN, STK37 | 607505 |