ID: 5814 | purine rich element binding protein B [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (44876299..44885530, complement) | PURBETA | 608887 |
ID: 6723 | spermidine synthase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (11054589..11060018, complement) | PAPT, SPDSY, SPS1L1, SRM | 182891 |
ID: 144699 | F-box and leucine rich repeat protein 14 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (1565993..1594842, complement) | Fbl14 | 609081 |
ID: 79939 | solute carrier family 35 member E1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (16549837..16572415, complement) | | 620337 |
ID: 6733 | SRSF protein kinase 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (105114740..105399357, complement) | SFRSK2 | 602980 |
ID: 116113 | forkhead box P4 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (41546381..41602384) | hFKHLA | 608924 |
ID: 23387 | SIK family kinase 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116843402..117098428, complement) | L19, QSK, SEMDK, SIK-3 | 614776 |
ID: 2289 | FKBP prolyl isomerase 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (35573590..35728583, complement) | AIG61, FKBP54, P54, PPIase, Ptg-10, FKBP5 | 602623 |
ID: 116983 | ArfGAP with coiled-coil, ankyrin repeat and PH domains 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (1292391..1307930, complement) | CENTB5 | |
ID: 6780 | staufen double-stranded RNA binding protein 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49113339..49219295, complement) | PPP1R150, STAU | 601716 |
ID: 9267 | cytohesin 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78674048..78782273, complement) | B2-1, CYTOHESIN-1, D17S811E, PSCD1, SEC7 | 182115 |
ID: 3150 | high mobility group nucleosome binding domain 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39342315..39349088, complement) | HMG14 | 163920 |
ID: 22976 | PAX interacting protein 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (154943690..155003411, complement) | CAGF28, CAGF29, PACIP1L, PTIP, TNRC2, PAXIP1 | 608254 |
ID: 9589 | WT1 associated protein [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (159726693..159756319) | Mum2 | 605442 |
ID: 54165 | defective in cullin neddylation 1 domain containing 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182938074..182985918, complement) | DCNL1, DCUN1L1, RP42, SCCRO, SCRO, Tes3 | 605905 |