ID: 245973 | ATPase H+ transporting V1 subunit C2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (10720943..10785110) | ATP6C2, VMA5 | 618070 |
ID: 4609 | MYC proto-oncogene, bHLH transcription factor [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (127735434..127742951) | MRTLC, bHLHe39, c-Myc, MYC | 190080 |
ID: 5080 | paired box 6 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (31789026..31817961, complement) | AN, AN1, AN2, ASGD5, D11S812E, FVH1, MGDA, WAGR | 607108 |
ID: 2534 | FYN proto-oncogene, Src family tyrosine kinase [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (111660332..111873452, complement) | SLK, SYN, p59-FYN | 137025 |
ID: 5966 | REL proto-oncogene, NF-kB subunit [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (60881574..60931612) | C-Rel, HIVEN86A, IMD92 | 164910 |
ID: 1230 | C-C motif chemokine receptor 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (46201711..46208313, complement) | CD191, CKR-1, CKR1, CMKBR1, HM145, MIP1aR, SCYAR1 | 601159 |
ID: 1158 | creatine kinase, M-type [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45306413..45322875, complement) | CKMM, CPK-M, M-CK | 123310 |
ID: 7443 | VRK serine/threonine kinase 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96797382..96881609) | HMNR10, PCH1, PCH1A | 602168 |
ID: 11235 | programmed cell death 10 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (167683298..167734892, complement) | CCM3, TFAR15 | 609118 |
ID: 2801 | golgin A2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128255829..128276007, complement) | DEDHMB, GM130 | 602580 |
ID: 8936 | WASP family member 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (110099819..110179670, complement) | NEDALVS, SCAR1, WAVE, WAVE1 | 605035 |
ID: 525 | ATPase H+ transporting V1 subunit B1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70935900..70965431) | ATP6B1, DRTA2, RTA1B, VATB, VMA2, VPP3 | 192132 |
ID: 523 | ATPase H+ transporting V1 subunit A [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (113747035..113812056) | ARCL2D, ATP6A11, DEE93, HO68, IECEE3, VA68, VPP2, Vma1, ATP6V1A | 607027 |
ID: 9341 | vesicle associated membrane protein 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (7771296..7781432) | CEB | 603657 |
ID: 8428 | serine/threonine kinase 24 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (98445185..98577107, complement) | HEL-S-95, MST3, MST3B, STE20, STK3 | 604984 |
ID: 526 | ATPase H+ transporting V1 subunit B2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (20197381..20221696) | ATP6B1B2, ATP6B2, DOOD, HO57, VATB, VPP3, Vma2, ZLS2 | 606939 |
ID: 4223 | mesenchyme homeobox 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (15611212..15686683, complement) | GAX, MOX2 | 600535 |
ID: 10953 | translocase of outer mitochondrial membrane 34 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (44942130..44960397, complement) | HTOM34P, TOM34, URCC3 | 616049 |
ID: 25831 | HECT domain E3 ubiquitin protein ligase 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (31100117..31207793, complement) | EULIR | 618649 |
ID: 529 | ATPase H+ transporting V1 subunit E1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (17592136..17628822, complement) | ARCL2C, ATP6E, ATP6E2, ATP6V1E, P31, Vma4 | 108746 |