ID: 9312 | potassium voltage-gated channel subfamily B member 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (72537225..72938349) | KV2.2 | 607738 |
ID: 135152 | beta-1,3-glucuronyltransferase 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (70856679..70957060, complement) | GLCATS | 607497 |
ID: 221938 | monocyte to macrophage differentiation associated 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (4892245..4959187, complement) | PAQR10 | 614581 |
ID: 219409 | GS homeobox 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27792483..27794768) | GSH1, Gsh-1 | 616542 |
ID: 27092 | calcium voltage-gated channel auxiliary subunit gamma 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66964707..67033398) | | 606404 |
ID: 55879 | gamma-aminobutyric acid type A receptor subunit theta [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152637895..152658965) | THETA | 300349 |
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: 112724 | retinol dehydrogenase 13 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (55039103..55069520, complement) | SDR7C3 | |
ID: 9892 | synaptosome associated protein 91 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (83552885..83709393, complement) | AP180, CALM | 607923 |
ID: 65009 | NDRG family member 4 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (58463715..58515387) | BDM1, SMAP-8, SMAP8 | 614463 |
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: 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: 9699 | regulating synaptic membrane exocytosis 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (103500610..104256094) | CRSDS, OBOE, RAB3IP3, RIM2 | 606630 |
ID: 29944 | PNMA family member 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (153056470..153060462) | MA3, MA5 | 300675 |
ID: 84258 | synaptotagmin 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (50621977..50658105, complement) | SytIII | 600327 |
ID: 9715 | family with sequence similarity 131 member B [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (143353400..143382304, complement) | | 619282 |
ID: 284339 | transmembrane protein 145 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (42313309..42325064) | | |
ID: 55964 | septin 3 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41969443..41998221) | SEP3, SEPT3, bK250D10.3 | 608314 |
ID: 286183 | sodium/potassium transporting ATPase interacting 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (62248854..62999652) | FAM77D-IT1, UG0898H09, NKAIN3 | 612872 |