ID: 22932 | POM121 and ZP3 fusion [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (76609986..76627279, complement) | POM-ZP3 | 600587 |
ID: 55100 | WD repeat domain 70 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (37379318..37753435) | | 617233 |
ID: 1889 | endothelin converting enzyme 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (21217250..21345504, complement) | ECE | 600423 |
ID: 5757 | prothymosin alpha [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (231708525..231713551) | TMSA | 188390 |
ID: 221960 | CCZ1 homolog B, vacuolar protein trafficking and biogenesis associated [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (6798937..6826275, complement) | C7orf28A, C7orf28B, CCZ1, H_NH0577018.2 | |
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: 220988 | heterogeneous nuclear ribonucleoprotein A3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (177212794..177223959) | 2610510D13Rik, D10S102, FBRNP, HNRPA3 | 605372 |
ID: 100289561 | uncharacterized LOC100289561 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (102363883..102380633) | | |
ID: 2288 | FKBP prolyl isomerase 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (2794970..2805423) | FKBP51, FKBP52, FKBP59, HBI, Hsp56, PPIase, p52 | 600611 |
ID: 10362 | high mobility group 20B [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3572944..3579083) | BRAF25, BRAF35, HMGX2, HMGXB2, PP7706, SMARCE1r, SOXL, pp8857 | 605535 |
ID: 728661 | solute carrier family 35 member E2B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (1661478..1692795, complement) | SLC35E2 | 619315 |
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: 54914 | focadhesin [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (20655625..20995950) | KIAA1797, SCOLIV | 614606 |
ID: 400566 | ligand of ATE1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (410325..414666) | C17orf97, CK20 | |
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: 81488 | RNA polymerase II subunit M [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (57706714..57717557) | GCOM1, GRINL1A, Gdown, Gdown1 | 606485 |
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: 23309 | SIN3 transcription regulator family member B [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (16829398..16880349) | | 607777 |
ID: 2879 | glutathione peroxidase 4 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (1103994..1106779) | GPx-4, GSHPx-4, MCSP, PHGPx, SMDS, snGPx, snPHGPx | 138322 |
ID: 57761 | tribbles pseudokinase 3 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (380760..397559) | C20orf97, NIPK, SINK, SKIP3, TRB3 | 607898 |