ID: 10005 | acyl-CoA thioesterase 8 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45841721..45857392, complement) | HNAACTE, NAP1, PTE-1, PTE-2, PTE1, PTE2, hACTE-III, hTE | 608123 |
ID: 2099 | estrogen receptor 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (151656672..152129619) | ER, ESR, ESRA, ESTRR, Era, NR3A1 | 133430 |
ID: 672 | BRCA1 DNA repair associated [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43044295..43170327, complement) | BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4, PPP1R53, PSCP, RNF53 | 113705 |
ID: 1080 | CF transmembrane conductance regulator [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117480025..117668665) | ABC35, ABCC7, CF/MRP, MRP7, TNR-CFTR, dJ760C5.1, CFTR | 602421 |
ID: 4137 | microtubule associated protein tau [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45894554..46028334) | DDPAC, FTD1, FTDP-17L, MSTD, MTBT1, MTBT2, PPND, PPP1R103, TAU, Tau-PHF6, tau-40, MAPT | 157140 |
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: 2908 | nuclear receptor subfamily 3 group C member 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (143277931..143435512, complement) | GCCR, GCR, GCRST, GR, GRL | 138040 |
ID: 3630 | insulin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2159779..2161209, complement) | IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10, PNDM4 | 176730 |
ID: 203228 | C9orf72-SMCR8 complex subunit [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (27546546..27573866, complement) | ALSFTD, DENND9, DENNL72, FTDALS, FTDALS1 | 614260 |
ID: 5371 | PML nuclear body scaffold [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (73994716..74047827) | MYL, PP8675, RNF71, TRIM19 | 102578 |
ID: 847 | catalase [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (34438934..34472060) | | 115500 |
ID: 5245 | prohibitin 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49404052..49414882, complement) | BAP32, HEL-215, HEL-S-54e, PHB | 176705 |
ID: 9636 | ISG15 ubiquitin like modifier [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (1013497..1014540) | G1P2, IFI15, IMD38, IP17, UCRP, hUCRP | 147571 |
ID: 8452 | cullin 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (224470150..224585363, complement) | CUL-3, NEDAUS, PHA2E | 603136 |
ID: 290 | alanyl aminopeptidase, membrane [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (89784895..89814852, complement) | AP-M, AP-N, APN, CD13, GP150, LAP1, P150, PEPN, hAPN | 151530 |
ID: 7846 | tubulin alpha 1a [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (49184795..49189080, complement) | B-ALPHA-1, LIS3, TUBA3 | 602529 |
ID: 6872 | TATA-box binding protein associated factor 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71366357..71530525) | BA2R, CCG1, CCGS, DYT3, DYT3/TAF1, KAT4, MRXS33, N-TAF1, NSCL2, OF, P250, TAF(II)250, TAF2A, TAFII-250, TAFII250, XDP | 313650 |
ID: 5966 | REL proto-oncogene, NF-kB subunit [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (60881574..60931612) | C-Rel, HIVEN86A, IMD92 | 164910 |
ID: 5160 | pyruvate dehydrogenase E1 subunit alpha 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (19343927..19361718) | E1alpha, PDHA, PDHAD, PDHCE1A, PHE1A | 300502 |
ID: 6045 | ring finger protein 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (185045558..185102603) | BAP-1, BAP1, DING, HIPI3, LUSYAM, RING1B, RING2 | 608985 |