ID: 79621 | ribonuclease H2 subunit B [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50909678..50970460) | AGS2, DLEU8 | 610326 |
ID: 675 | BRCA2 DNA repair associated [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (32315077..32400268) | BRCC2, BROVCA2, FACD, FAD, FAD1, FANCD, FANCD1, GLM3, PNCA2, XRCC11 | 600185 |
ID: 142 | poly(ADP-ribose) polymerase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (226360691..226408093, complement) | ADPRT, ADPRT 1, ADPRT1, ARTD1, PARP, PARP-1, PARS, PPOL, Poly-PARP, pADPRT-1 | 173870 |
ID: 5925 | RB transcriptional corepressor 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (48303751..48481890) | OSRC, PPP1R130, RB, p105-Rb, p110-RB1, pRb, pp110 | 614041 |
ID: 7490 | WT1 transcription factor [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (32387775..32435539, complement) | AWT1, GUD, NPHS4, WAGR, WIT-2, WT-1, WT33 | 607102 |
ID: 100874255 | RNASEH2B antisense RNA 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50882378..50910712, complement) | | |
ID: 2305 | forkhead box M1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (2857680..2877174, complement) | FKHL16A, FOXM1B, FOXM1C, HFH-11, HFH11, HNF-3, INS-1, MPHOSPH2, MPP-2, MPP2, PIG29, TRIDENT, FOXM1 | 602341 |
ID: 11200 | checkpoint kinase 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (28687743..28741834, complement) | CDS1, CHK2, HuCds1, LFS2, PP1425, RAD53, TPDS4, hCds1 | 604373 |
ID: 5295 | phosphoinositide-3-kinase regulatory subunit 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (68215756..68301821) | AGM7, GRB1, IMD36, p85, p85-ALPHA, p85alpha | 171833 |
ID: 2022 | endoglin [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127815016..127854658, complement) | END, HHT1, ORW1 | 131195 |
ID: 4893 | NRAS proto-oncogene, GTPase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (114704469..114716771, complement) | ALPS4, CMNS, KRAS, N-ras, NCMS1, NS6, NRAS | 164790 |
ID: 3014 | H2A.X variant histone [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (119093874..119095465, complement) | H2A.X, H2A/X, H2AFX | 601772 |
ID: 103 | adenosine deaminase RNA specific [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (154582057..154627997, complement) | ADAR1, AGS6, DRADA, DSH, DSRAD, G1P1, IFI-4, IFI4, K88DSRBP, P136 | 146920 |
ID: 2194 | fatty acid synthase [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (82078338..82098236, complement) | FAS, OA-519, SDR27X1 | 600212 |
ID: 6117 | replication protein A1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (1830005..1900082) | HSSB, MST075, PFBMFT6, REPA1, RF-A, RP-A, RPA70 | 179835 |
ID: 4067 | LYN proto-oncogene, Src family tyrosine kinase [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (55879835..56014169) | JTK8, SAIDV, p53Lyn, p56Lyn | 165120 |
ID: 8350 | H3 clustered histone 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (26020451..26020958) | H3/A0, H3C11, H3C12, H3C2, H3C3, H3C4, H3C6, H3C7, H3C8, H3FA, HIST1H3A, H3C1 | 602810 |
ID: 10971 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (9583967..9630997, complement) | 14-3-3, 1C5, HS1 | 609009 |
ID: 8473 | O-linked N-acetylglucosamine (GlcNAc) transferase [Homo sapiens (human)] | Chromosome X, NC_000023.11 (71533104..71575892) | HINCUT-1, HRNT1, MRX106, O-GLCNAC1, XLID106, OGT | 300255 |
ID: 57674 | ring finger protein 213 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80260852..80398794) | ALO17, C17orf27, KIAA1618, MYMY2, MYSTR, NET57 | 613768 |