ID: 6538 | solute carrier family 6 member 11 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (10816228..10940714) | GAT-3, GAT3, GAT4 | 607952 |
ID: 22865 | SLIT and NTRK like family member 3 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (165186720..165197109, complement) | | 609679 |
ID: 9892 | synaptosome associated protein 91 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (83552885..83709393, complement) | AP180, CALM | 607923 |
ID: 57699 | copine 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (36740775..36839998, complement) | COPN5, CPN5 | 604209 |
ID: 3084 | neuregulin 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (31639245..32774046) | ARIA, GGF, GGF2, HGL, HRG, HRG1, HRGA, MST131, MSTP131, NDF-IT2, SMDF, NRG1 | 142445 |
ID: 50801 | potassium two pore domain channel subfamily K member 4 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (64291302..64300031) | FHEIG, K2p4.1, TRAAK, TRAAK1 | 605720 |
ID: 259236 | transmembrane inner ear [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (46693778..46710886) | DFNB6 | 607237 |
ID: 9312 | potassium voltage-gated channel subfamily B member 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (72537225..72938349) | KV2.2 | 607738 |
ID: 7101 | nuclear receptor subfamily 2 group E member 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (108166022..108188809) | TLL, TLX, XTLL | 603849 |
ID: 4744 | neurofilament heavy chain [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29480218..29491390) | CMT2CC, NFH | 162230 |
ID: 6861 | synaptotagmin 5 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (55171196..55180289, complement) | | 600782 |
ID: 5458 | POU class 4 homeobox 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (146638893..146642474) | BRN3.2, BRN3B, Brn-3b | 113725 |
ID: 6506 | solute carrier family 1 member 2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (35251205..35420507, complement) | DEE41, EAAT2, EIEE41, GLT-1, GLT1, HBGT | 600300 |
ID: 221938 | monocyte to macrophage differentiation associated 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (4892245..4959187, complement) | PAQR10 | 614581 |
ID: 116986 | ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (57723761..57742161, complement) | CENTG1, GGAP2, PIKE | 605476 |
ID: 283576 | zinc finger DHHC-type palmitoyltransferase 22 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (77131270..77142288, complement) | C14orf59 | |
ID: 219409 | GS homeobox 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27792483..27794768) | GSH1, Gsh-1 | 616542 |
ID: 27344 | proprotein convertase subtilisin/kexin type 1 inhibitor [Homo sapiens (human)] | Chromosome X, NC_000023.11 (48831096..48835610, complement) | BigLEN, PEN, PROSAAS, SAAS, SCG8, SgVIII | 300399 |
ID: 121643 | forkhead box N4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109277978..109309284, complement) | | 609429 |
ID: 27087 | beta-1,3-glucuronyltransferase 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (134378504..134412242, complement) | CD57, GLCATP, GLCUATP, HNK1, LEU7, NK-1, NK1 | 151290 |