ID: 4913 | nth like DNA glycosylase 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2039820..2047834, complement) | FAP3, NTH1, OCTS3, hNTH1 | 602656 |
ID: 7249 | TSC complex subunit 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2047985..2089491) | LAM, PPP1R160, TSC4 | 191092 |
ID: 56890 | Mdm1 nuclear protein [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (68294566..68332362, complement) | | 613813 |
ID: 9611 | nuclear receptor corepressor 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16029157..16215534, complement) | N-CoR, N-CoR1, PPP1R109, TRAC1, hN-CoR | 600849 |
ID: 23144 | zinc finger CCCH-type containing 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143437659..143541447, complement) | SMICL, ZC3HDC3 | 618640 |
ID: 197342 | essential meiotic structure-specific endonuclease subunit 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1772810..1781702) | SLX2B, gs125 | 610886 |
ID: 26502 | nuclear prelamin A recognition factor [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (82458198..82490537) | IOP2 | 605349 |
ID: 8650 | NUMB endocytic adaptor protein [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (73275216..73458546, complement) | C14orf41, S171, c14_5527 | 603728 |
ID: 140459 | ankyrin repeat and SOCS box containing 6 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (129634605..129642151, complement) | | 615051 |
ID: 253512 | solute carrier family 25 member 30 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (45393316..45434016, complement) | KMCP1 | 610793 |
ID: 387893 | lysine methyltransferase 5A [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123384132..123409353) | PR-Set7, PR/SET07, SET07, SET8, SETD8 | 607240 |
ID: 4521 | nudix hydrolase 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (2242226..2251145) | MTH1 | 600312 |
ID: 55824 | phosphoprotein membrane anchor with glycosphingolipid microdomains 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (80967810..81112068, complement) | CBP, PAG | 605767 |
ID: 64146 | peptide deformylase, mitochondrial [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69326913..69330588, complement) | | 618720 |
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: 29960 | mitochondrial rRNA methyltransferase 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (2234195..2242205, complement) | FJH1, FTSJ2, HEL97, MTDPS17, RRMJ2 | 606906 |
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: 25897 | ring finger protein 19A, RBR E3 ubiquitin protein ligase [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (100257067..100336204, complement) | RNF19 | 607119 |
ID: 2235 | ferrochelatase [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (57544377..57586702, complement) | EPP, EPP1, FCE | 612386 |
ID: 8508 | nipsnap homolog 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29554808..29581113, complement) | | 603249 |