ID: 2651 | glucosaminyl (N-acetyl) transferase 2 (I blood group) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (10521351..10629368) | CCAT, CTRCT13C, GCNT5, IGNT, II, NACGT1, NAGCT1, ULG3, bA360O19.2, bA421M1.1, GCNT2 | 600429 |
ID: 5071 | parkin RBR E3 ubiquitin protein ligase [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (161347417..162727766, complement) | AR-JP, LPRS2, PARK2, PDJ | 602544 |
ID: 648 | BMI1 proto-oncogene, polycomb ring finger [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (22321099..22331706) | FLVI2/BMI1, PCGF4, RNF51, flvi-2/bmi-1 | 164831 |
ID: 644378 | GCNT2 pseudogene 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (10633760..10634830) | GCNT2P, GCNT6 | |
ID: 3115 | major histocompatibility complex, class II, DP beta 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (33075990..33089696) | DPB1, HLA-DP, HLA-DP1B, HLA-DPB | 142858 |
ID: 7248 | TSC complex subunit 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (132891349..132945378, complement) | LAM, TSC | 605284 |
ID: 8451 | cullin 4A [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113208193..113267108) | | 603137 |
ID: 6929 | transcription factor 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (1609292..1652615, complement) | AGM8, AGM8A, AGM8B, E2A, E47, ITF1, TCF-3, VDIR, bHLHb21, p75 | 147141 |
ID: 3184 | heterogeneous nuclear ribonucleoprotein D [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (82352498..82373991, complement) | AUF1, AUF1A, HNRPD, P37, hnRNPD0 | 601324 |
ID: 375 | ARF GTPase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (228082708..228099212) | PVNH8 | 103180 |
ID: 1487 | C-terminal binding protein 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (1211445..1250355, complement) | BARS, HADDTS | 602618 |
ID: 7706 | tripartite motif containing 25 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (56887909..56914049, complement) | EFP, RNF147, Z147, ZNF147 | 600453 |
ID: 406976 | microRNA 199a-1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10817426..10817496, complement) | MIR-199-s, MIRN199A1, mir-199a-1 | 610719 |
ID: 10498 | coactivator associated arginine methyltransferase 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10871553..10923075) | PRMT4 | 603934 |
ID: 253260 | RPTOR independent companion of MTOR complex 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (38937920..39074399, complement) | AVO3, PIA, hAVO3 | 609022 |
ID: 84447 | synoviolin 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65127279..65134519, complement) | DER3, HRD1 | 608046 |
ID: 3187 | heterogeneous nuclear ribonucleoprotein H1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (179614178..179634784, complement) | HNRPH, HNRPH1, NEDCDS, hnRNPH | 601035 |
ID: 5861 | RAB1A, member RAS oncogene family [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (65086854..65130106, complement) | RAB1, YPT1 | 179508 |
ID: 8570 | KH-type splicing regulatory protein [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (6413102..6424811, complement) | FBP2, FUBP2, KSRP, p75 | 603445 |
ID: 79718 | TBL1X/Y related 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (177019344..177201800, complement) | C21, DC42, IRA1, MRD41, TBLR1 | 608628 |