ID: 55599 | RNA binding region (RNP1, RRM) containing 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (103525699..103555239) | CPHD7, IGHD5, RBM40, RNP, SNRNP65 | 618016 |
ID: 92482 | BBSome interacting protein 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (110898730..110919366, complement) | BBIP10, BBS18, NCRNA00081, bA348N5.3 | 613605 |
ID: 84081 | nuclear speckle splicing regulatory protein 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30116816..30186475) | CCDC55, HSPC095, NEDSSBA, NSrp70 | 616173 |
ID: 57122 | nucleoporin 107 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (68686978..68745809) | NPHS11, NUP84, ODG6, ODG6; GAMOS7 | 607617 |
ID: 23215 | proline rich coiled-coil 2C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (171485530..171593511) | BAT2-iso, BAT2D1, BAT2L2, XTP2 | 617373 |
ID: 26268 | F-box protein 9 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (53064998..53100873) | FBX9, NY-REN-57, VCIA1, dJ341E18.2 | 609091 |
ID: 283237 | tetratricopeptide repeat domain 9C [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (62728049..62738636) | | |
ID: 57697 | FA complementation group M [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (45135930..45200890) | FAAP250, KIAA1596, POF15, SPGF28 | 609644 |
ID: 5527 | protein phosphatase 2 regulatory subunit B'gamma [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (101760573..101927992) | B56G, B56gamma, PR61G | 601645 |
ID: 91750 | lin-52 DREAM MuvB core complex component [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74084956..74201493) | C14orf46, c14_5549 | |
ID: 11340 | exosome component 8 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (37000786..37009614) | CIP3, EAP2, OIP2, PCH1C, RRP43, Rrp43p, bA421P11.3, p9 | 606019 |
ID: 9277 | WD repeat domain 46 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (33279108..33289239, complement) | BING4, C6orf11, FP221, UTP7 | 611440 |
ID: 84292 | WD repeat domain 83 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12666807..12675832) | MORG1 | 616850 |
ID: 51398 | WD repeat domain 83 opposite strand [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12668073..12669415, complement) | ASTERIX, C19orf56, PAT-10, PAT10, PTD008 | 618474 |
ID: 9937 | DNA cross-link repair 1A [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (113834725..113854394, complement) | PSO2, SNM1, SNM1A | 609682 |
ID: 9777 | transmembrane 9 superfamily member 4 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32109714..32167256) | dJ836N17.2 | 617727 |
ID: 6203 | ribosomal protein S9 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (54200858..54207647) | S9, uS4 | 603631 |
ID: 11120 | butyrophilin subfamily 2 member A1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (26457955..26476622) | BK14H9.1, BT2.1, BTF1, BTN2.1, DJ3E1.1 | 613590 |
ID: 84316 | N-alpha-acetyltransferase 38, NatC auxiliary subunit [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7856685..7885420, complement) | LSMD1, MAK31, PFAAP2 | 617990 |
ID: 55702 | YJU2 splicing factor homolog [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (4247080..4269088) | CCDC94 | |