ID: 381 | ARF GTPase 5 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (127588411..127591700) | | 103188 |
ID: 23039 | exportin 7 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (21919662..22006585) | EXP7, RANBP16 | 606140 |
ID: 6227 | ribosomal protein S21 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (62387103..62388520) | HLDF, S21, eS21 | 180477 |
ID: 522 | ATP synthase peripheral stalk subunit F6 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (25724500..25735653, complement) | ATP5, ATP5A, ATP5J, ATPM, CF6, F6 | 603152 |
ID: 78996 | cell cycle regulator of NHEJ [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (135092303..135172469, complement) | C7orf49-1, CYREN-2, MRI, MRI-2, CYREN | 616980 |
ID: 7267 | tetratricopeptide repeat domain 3 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37073254..37203118) | DCRR1, RNF105, TPRDIII | 602259 |
ID: 56882 | CDC42 small effector 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151050985..151059622, complement) | SCIP1, SPEC1 | 619456 |
ID: 533 | ATPase H+ transporting V0 subunit b [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43974960..43978295) | ATP6F, HATPL, VMA16 | 603717 |
ID: 10616 | RANBP2-type and C3HC4-type zinc finger containing 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (408299..432139) | C20orf18, HOIL-1, HOIL1, PBMEI, PGBM1, RBCK2, RNF54, UBCE7IP3, XAP3, XAP4, ZRANB4 | 610924 |
ID: 79959 | centrosomal protein 76 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (12661956..12702777, complement) | C18orf9, HsT1705 | 620791 |
ID: 84262 | proteasome assembly chaperone 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (1567332..1570032, complement) | C7orf48, PAC3 | 617528 |
ID: 79627 | opioid growth factor receptor like 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (71288811..71309059) | dJ331H24.1 | |
ID: 83707 | tRNA phosphotransferase 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (64223799..64226257, complement) | | 610470 |
ID: 10962 | MLLT11 transcription factor 7 cofactor [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151060397..151069544) | AF1Q | 604684 |
ID: 84304 | nudix hydrolase 22 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (64226258..64230269) | | |
ID: 55780 | ER membrane associated RNA degradation [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (169751306..169781600) | C6orf70, PVNH6, dJ266L20.3 | 615532 |
ID: 5976 | UPF1 RNA helicase and ATPase [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (18831959..18868230) | HUPF1, NORF1, RENT1, UTF, pNORF1, smg-2 | 601430 |
ID: 63916 | engulfment and cell motility 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (46366050..46406615, complement) | CED-12, CED12, Ced-12A, ELMO-2, VMPI | 606421 |
ID: 10155 | tripartite motif containing 28 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (58544064..58550715) | KAP1, PPP1R157, RNF96, TF1B, TIF1B, TIF1beta | 601742 |
ID: 80772 | ceramide-1-phosphate transfer protein [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (1324802..1328896) | GLTPD1 | 615467 |