ID: 100507462 | CCDC28A antisense RNA 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (138725215..138773703, complement) | GVQW2 | |
ID: 100506804 | TMEM30A divergent transcript [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (75285014..75291864) | | |
ID: 100506409 | ELOVL2 antisense RNA 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (11043758..11079144) | | |
ID: 317671 | Rieske Fe-S domain containing [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (95646777..95658082) | | |
ID: 165055 | coiled-coil domain containing 138 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (108786750..108885485) | | |
ID: 147184 | KRT10 antisense RNA 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (40819145..40836274) | TMEM99 | |
ID: 117177 | RAB3A interacting protein [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (69738242..69823204) | RABIN3, RABIN8 | 608686 |
ID: 90141 | EF-hand calcium binding domain 11 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (89794669..89954777, complement) | C14orf143 | |
ID: 79977 | grainyhead like transcription factor 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (101492439..101681200) | BOM, DFNA28, ECTDS, PPCD4, TFCP2L3 | 608576 |
ID: 51377 | ubiquitin C-terminal hydrolase L5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (193012254..193060076, complement) | CGI-70, INO80R, UCH-L5, UCH37 | 610667 |
ID: 26520 | translocase of inner mitochondrial membrane 9 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (58408494..58427531, complement) | TIM9, TIM9A | 607384 |
ID: 25898 | ring finger and CHY zinc finger domain containing 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (75479033..75514715, complement) | ARNIP, CHIMP, PIRH2, PRO1996, RNF199, ZCHY, ZNF363 | 607680 |
ID: 23783 | ANKRD62P1-PARP4P3 readthrough, transcribed pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (16653708..16675540, complement) | VWFP1-ANKRD62P1-PARP4P3 | |
ID: 23347 | structural maintenance of chromosomes flexible hinge domain containing 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2655726..2805017) | BAMS, FSHD2 | 614982 |
ID: 11098 | serine protease 23 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (86791071..86952910) | SIG13, SPUVE, ZSIG13 | 618376 |
ID: 10617 | STAM binding protein [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (73828961..73873656) | AMSH, MICCAP | 606247 |
ID: 9141 | programmed cell death 5 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32581190..32587453) | TFAR19 | 604583 |
ID: 8089 | YEATS domain containing 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (69359743..69427072) | 4930573H17Rik, B230215M10Rik, GAS41, NUBI-1, YAF9 | 602116 |
ID: 6993 | dynein light chain Tctex-type 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (158636474..158644743, complement) | CW-1, TCTEL1, TCTEX1, tctex-1 | 601554 |
ID: 6728 | signal recognition particle 19 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (112861287..112898371) | | 182175 |