ID: 80344 | DDB1 and CUL4 associated factor 11 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (24114777..24125242) | GL014, PRO2389, WDR23 | 613317 |
ID: 10363 | high mobility group 20A [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (77420888..77520050) | HMGX1, HMGXB1 | 605534 |
ID: 57697 | FA complementation group M [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (45135930..45200890) | FAAP250, KIAA1596, POF15, SPGF28 | 609644 |
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: 84081 | nuclear speckle splicing regulatory protein 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30116816..30186475) | CCDC55, HSPC095, NEDSSBA, NSrp70 | 616173 |
ID: 91750 | lin-52 DREAM MuvB core complex component [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74084956..74201493) | C14orf46, c14_5549 | |
ID: 55035 | nucleolar protein 8 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (92297358..92325350, complement) | C9orf34, NOP132, bA62C3.3, bA62C3.4 | 611534 |
ID: 29088 | mitochondrial ribosomal protein L15 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (54135241..54148514) | HSPC145, L15mt, MRP-L15, MRP-L7, RPML7, uL15m | 611828 |
ID: 374354 | NHL repeat containing 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (113854661..113917194) | FINCA | 618277 |
ID: 23645 | protein phosphatase 1 regulatory subunit 15A [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (48872421..48876058) | GADD34 | 611048 |
ID: 4659 | protein phosphatase 1 regulatory subunit 12A [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (79773563..79935460, complement) | GUBS, M130, MBS, MYPT1 | 602021 |
ID: 10229 | coenzyme Q7, hydroxylase [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (19067614..19083097) | CAT5, CLK-1, CLK1, COQ10D8, HMNR9 | 601683 |
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: 2521 | FUS RNA binding protein [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (31180110..31194871) | ALS6, ETM41, HNRNPP2, POMP75, TLS, altFUS, FUS | 137070 |
ID: 92482 | BBSome interacting protein 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (110898730..110919366, complement) | BBIP10, BBS18, NCRNA00081, bA348N5.3 | 613605 |
ID: 55778 | zinc finger protein 839 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (102317506..102342367) | C14orf131 | |
ID: 56254 | ring finger protein 20 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (101533853..101563344) | BRE1, BRE1A, hBRE1 | 607699 |
ID: 28981 | intraflagellar transport 81 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110124357..110218793) | CDV-1, CDV-1R, CDV1, CDV1R, DV1, SRTD19 | 605489 |
ID: 91574 | mitochondrial translation release factor in rescue [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123232914..123257960) | C12orf65, COXPD7, SPG55, mtRF-R | 613541 |