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: 55100 | WD repeat domain 70 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (37379318..37753435) | | 617233 |
ID: 199870 | family with sequence similarity 76 member A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (27725961..27763116) | | |
ID: 10096 | actin related protein 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (113889934..113962596) | ARP3 | 604222 |
ID: 151987 | protein phosphatase 4 regulatory subunit 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (72996743..73069198) | PP4R2 | 613822 |
ID: 10865 | AT-rich interaction domain 5A [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (96536752..96552638) | MRF-1, MRF1, RP11-363D14 | 611583 |
ID: 2033 | E1A binding protein p300 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41092592..41180077) | KAT3B, MKHK2, RSTS2, p300 | 602700 |
ID: 84769 | MPV17 mitochondrial inner membrane protein like 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (18193218..18196948) | FKSG24 | 616133 |
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: 51719 | calcium binding protein 39 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (230712842..230821075) | CGI-66, MO25 | 612174 |
ID: 10921 | RNA binding protein with serine rich domain 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2253116..2268126, complement) | E5.1 | 606447 |
ID: 728661 | solute carrier family 35 member E2B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (1661478..1692795, complement) | SLC35E2 | 619315 |
ID: 27032 | ATPase secretory pathway Ca2+ transporting 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (130850595..131016712) | ATP2C1A, BCPM, HHD, PMR1, SPCA1, hSPCA1 | 604384 |
ID: 84971 | autophagy related 4D cysteine peptidase [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10543904..10553418) | APG4-D, APG4D, AUTL4, HsAPG4D | 611340 |
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: 9807 | inositol hexakisphosphate kinase 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49724294..49786542, complement) | IHPK1, PiUS | 606991 |
ID: 2181 | acyl-CoA synthetase long chain family member 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (222861036..222944639) | ACS3, FACL3, LACS 3, LACS3, PRO2194 | 602371 |
ID: 25862 | ubiquitin specific peptidase 49 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (41789896..41895375, complement) | | |
ID: 4084 | MAX dimerization protein 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (69915109..69942945) | BHLHC58, MAD, MAD1 | 600021 |