ID: 55510 | DEAD-box helicase 43 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (73394828..73417566) | CT13, HAGE | 606286 |
ID: 351 | amyloid beta precursor protein [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (25880550..26171128, complement) | AAA, ABETA, ABPP, AD1I, CTFgamma, CVAP, PN-II, PN2, alpha-sAPP, preA4, APP | 104760 |
ID: 3845 | KRAS proto-oncogene, GTPase [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (25205246..25250929, complement) | 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A, K-RAS4B, K-Ras, K-Ras 2, KI-RAS1, KRAS2, NS, NS3, OES, RALD, RASK2, c-Ki-ras, c-Ki-ras2, KRAS | 190070 |
ID: 4609 | MYC proto-oncogene, bHLH transcription factor [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (127735434..127742951) | MRTLC, bHLHe39, c-Myc, MYC | 190080 |
ID: 4000 | lamin A/C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156082573..156140081) | CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL, FPLD, FPLD2, HGPS, IDC, LDP1, LFP, LGMD1B, LMN1, LMNC, LMNL1, MADA, PRO1 | 150330 |
ID: 5747 | protein tyrosine kinase 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (140657900..141002079, complement) | FADK, FADK 1, FAK, FAK1, FRNK, PPP1R71, p125FAK, pp125FAK | 600758 |
ID: 283120 | H19 imprinted maternally expressed transcript [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (1995176..2001266, complement) | ASM, ASM1, BWS, D11S813E, LINC00008, MIR675HG, NCRNA00008, WT2 | 103280 |
ID: 1788 | DNA methyltransferase 3 alpha [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (25227874..25342590, complement) | DNMT3A2, HESJAS, M.HsaIIIA, TBRS | 602769 |
ID: 406962 | microRNA 186 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (71067631..71067716, complement) | MIRN186, miR-186 | |
ID: 7182 | nuclear receptor subfamily 2 group C member 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (14947583..15049273) | TAK1, TR4 | 601426 |
ID: 3187 | heterogeneous nuclear ribonucleoprotein H1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (179614178..179634784, complement) | HNRPH, HNRPH1, NEDCDS, hnRNPH | 601035 |
ID: 1665 | DEAH-box helicase 15 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (24527475..24584554, complement) | DBP1, DDX15, PRP43, PRPF43, PrPp43p, hPrp43 | 603403 |
ID: 3069 | high density lipoprotein binding protein [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241227291..241315672, complement) | HBP, PRO2900, VGL | 142695 |
ID: 6205 | ribosomal protein S11 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49496434..49499708) | S11, uS17 | 180471 |
ID: 3189 | heterogeneous nuclear ribonucleoprotein H3 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (68331693..68343196) | 2H9, HNRPH3 | 602324 |
ID: 26003 | golgi reassembly stacking protein 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (170928477..170967130) | GOLPH6, GRASP55, GRS2, p59 | 608693 |
ID: 168400 | DEAD-box helicase 53 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (22999960..23003589) | CAGE, CT26 | 301079 |
ID: 6787 | NIMA related kinase 4 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (52708444..52770940, complement) | NRK2, STK2, pp12301 | 601959 |
ID: 26094 | DDB1 and CUL4 associated factor 4 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (72926464..72962098) | WDR21, WDR21A | 616372 |
ID: 202559 | KH RNA binding domain containing, signal transduction associated 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (61542670..62286225, complement) | KHDRBS2-OT-OT1, SLM-1, SLM1, KHDRBS2 | 610487 |