ID: 5757 | prothymosin alpha [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (231708525..231713551) | TMSA | 188390 |
ID: 5223 | phosphoglycerate mutase 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (97426191..97433444) | HEL-S-35, PGAM-B, PGAMA | 172250 |
ID: 55100 | WD repeat domain 70 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (37379318..37753435) | | 617233 |
ID: 6142 | ribosomal protein L18a [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17859910..17863319) | L18A, eL20 | 604178 |
ID: 7923 | hydroxysteroid 17-beta dehydrogenase 8 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (33204655..33206831) | D6S2245E, FABG, FABGL, H2-KE6, HKE6, KE6, RING2, SDR30C1, dJ1033B10.9 | 601417 |
ID: 4849 | CCR4-NOT transcription complex subunit 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (54137762..54155681) | IDDSADF, LENG2, NOT3, NOT3H | 604910 |
ID: 64795 | required for meiotic nuclear division 5 homolog A [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (86720291..86778041) | CTLH, GID2, GID2A, RMD5, p44CTLH | 618964 |
ID: 22932 | POM121 and ZP3 fusion [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (76609986..76627279, complement) | POM-ZP3 | 600587 |
ID: 84769 | MPV17 mitochondrial inner membrane protein like 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (18193218..18196948) | FKSG24 | 616133 |
ID: 10865 | AT-rich interaction domain 5A [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (96536752..96552638) | MRF-1, MRF1, RP11-363D14 | 611583 |
ID: 4084 | MAX dimerization protein 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (69915109..69942945) | BHLHC58, MAD, MAD1 | 600021 |
ID: 84901 | nuclear factor of activated T cells 2 interacting protein [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (28950937..28967092) | ESC2, NIP45, RAD60 | 614525 |
ID: 25862 | ubiquitin specific peptidase 49 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (41789896..41895375, complement) | | |
ID: 55527 | fem-1 homolog A [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (4791734..4801273) | EPRAP | 613538 |
ID: 28989 | N-terminal Xaa-Pro-Lys N-methyltransferase 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (129608872..129636135) | AD-003, C9orf32, HOMT1A, METTL11A, NRMT, NRMT1, NTM1A | 613560 |
ID: 8897 | myotubularin related protein 3 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29883174..30030868) | FYVE-DSP1, ZFYVE10 | 603558 |
ID: 23067 | SET domain containing 1B, histone lysine methyltransferase [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (121790155..121832656) | IDDSELD, KMT2G, Set1B | 611055 |
ID: 10096 | actin related protein 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (113889934..113962596) | ARP3 | 604222 |
ID: 51463 | G protein-coupled receptor 89B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (147928420..148025934) | GPHR, GPR89, GPR89C, LINC02804, SH120, UNQ192 | 612806 |
ID: 51719 | calcium binding protein 39 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (230712842..230821075) | CGI-66, MO25 | 612174 |