ID: 84081 | nuclear speckle splicing regulatory protein 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30116816..30186475) | CCDC55, HSPC095, NEDSSBA, NSrp70 | 616173 |
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: 92482 | BBSome interacting protein 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (110898730..110919366, complement) | BBIP10, BBS18, NCRNA00081, bA348N5.3 | 613605 |
ID: 9937 | DNA cross-link repair 1A [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (113834725..113854394, complement) | PSO2, SNM1, SNM1A | 609682 |
ID: 91452 | acyl-CoA binding domain containing 5 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (27182838..27242111, complement) | RDLKD | 616618 |
ID: 80344 | DDB1 and CUL4 associated factor 11 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (24114777..24125242) | GL014, PRO2389, WDR23 | 613317 |
ID: 55702 | YJU2 splicing factor homolog [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (4247080..4269088) | CCDC94 | |
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: 55055 | zwilch kinetochore protein [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (66505326..66550130) | KNTC1AP, hZwilch | 609984 |
ID: 100996928 | FMC1-LUC7L2 readthrough [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (139341337..139423454) | C7orf55, C7orf55-LUC7L2, FMC1 | |
ID: 154791 | formation of mitochondrial complex V assembly factor 1 homolog [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (139340472..139346328) | C7orf55, HSPC268 | 620766 |
ID: 55035 | nucleolar protein 8 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (92297358..92325350, complement) | C9orf34, NOP132, bA62C3.3, bA62C3.4 | 611534 |
ID: 401541 | centromere protein P [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (92325468..92620529) | CENP-P | 611505 |
ID: 374354 | NHL repeat containing 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (113854661..113917194) | FINCA | 618277 |
ID: 10363 | high mobility group 20A [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (77420888..77520050) | HMGX1, HMGXB1 | 605534 |
ID: 26001 | ring finger protein 167 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (4940092..4945222) | 5730408C10Rik, LP2254, RING105 | 610431 |
ID: 9692 | protein only RNase P catalytic subunit [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (35121839..35277622) | COXPD54, KIAA0391, MRPP3 | 609947 |
ID: 57697 | FA complementation group M [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (45135930..45200890) | FAAP250, KIAA1596, POF15, SPGF28 | 609644 |
ID: 158293 | family with sequence similarity 120 member A opposite strand [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (93443332..93453601, complement) | C9orf10OS | |
ID: 55012 | protein phosphatase 2 regulatory subunit B''gamma [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (35085472..35122298, complement) | C14orf10, G4-1, G5pr, GDRM, MEGD, SPGF36 | 615902 |