ID: 137902 | peroxidasin like [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (51319577..51809445, complement) | PMR1, PRM1, VPO2 | 615904 |
ID: 348 | apolipoprotein E [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (44905796..44909393) | AD2, APO-E, ApoE4, LDLCQ5, LPG | 107741 |
ID: 4843 | nitric oxide synthase 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (27756766..27800529, complement) | HEP-NOS, INOS, NOSA, NOS2 | 163730 |
ID: 8452 | cullin 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (224470150..224585363, complement) | CUL-3, NEDAUS, PHA2E | 603136 |
ID: 1445 | C-terminal Src kinase [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (74782080..74803197) | | 124095 |
ID: 10498 | coactivator associated arginine methyltransferase 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10871553..10923075) | PRMT4 | 603934 |
ID: 6709 | spectrin alpha, non-erythrocytic 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128552587..128633662) | DEE5, DEVEP, EIEE5, HMN11, HMND11, NEAS, SPG91, SPTA2 | 182810 |
ID: 9318 | COP9 signalosome subunit 2 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (49122727..49155599, complement) | ALIEN, CSN2, SGN2, TRIP15 | 604508 |
ID: 2873 | G protein pathway suppressor 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (82050932..82057470) | COPS1, CSN1, SGN1 | 601934 |
ID: 26249 | kelch like family member 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (137617500..137736089, complement) | PHA2D | 605775 |
ID: 9790 | BMS1 ribosome biogenesis factor [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (42782795..42834937) | ACCL, BMS1 | 611448 |
ID: 79848 | centrosome and spindle pole associated protein 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (67064368..67196614) | CSPP, CSPP-L, JBTS21 | 611654 |
ID: 26578 | osteoclast stimulating factor 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (75088514..75147265) | OSF, SH3P2, bA235O14.1 | 610180 |
ID: 9886 | Rho related BTB domain containing 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (60860860..61001967, complement) | | 607351 |
ID: 121665 | signal peptide peptidase like 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (120762510..120904358, complement) | IMP2, MDHV1887, PRO4332, PSH1, PSL4 | 608240 |
ID: 84078 | kelch repeat and BTB domain containing 7 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41189834..41194569, complement) | | 617739 |
ID: 26051 | protein phosphatase 1 regulatory subunit 16B [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38805697..38923024) | ANKRD4, TIMAP | 613275 |
ID: 139189 | diacylglycerol kinase kappa [Homo sapiens (human)] | Chromosome X, NC_000023.11 (50365409..50470825, complement) | | 300837 |
ID: 79734 | potassium channel tetramerization domain containing 17 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37051742..37063390) | | 616386 |
ID: 51596 | cutA divalent cation tolerance homolog [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (33416442..33418107, complement) | ACHAP, C6orf82 | 616953 |