ID: 135152 | beta-1,3-glucuronyltransferase 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (70856679..70957060, complement) | GLCATS | 607497 |
ID: 9312 | potassium voltage-gated channel subfamily B member 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (72537225..72938349) | KV2.2 | 607738 |
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: 55879 | gamma-aminobutyric acid type A receptor subunit theta [Homo sapiens (human)] | Chromosome X, NC_000023.11 (152637895..152658965) | THETA | 300349 |
ID: 112724 | retinol dehydrogenase 13 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (55039103..55069520, complement) | SDR7C3 | |
ID: 6752 | somatostatin receptor 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (73165010..73176633) | SST2 | 182452 |
ID: 65009 | NDRG family member 4 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (58463715..58515387) | BDM1, SMAP-8, SMAP8 | 614463 |
ID: 286183 | sodium/potassium transporting ATPase interacting 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (62248854..62999652) | FAM77D-IT1, UG0898H09, NKAIN3 | 612872 |
ID: 10570 | dihydropyrimidinase like 4 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (132186948..132205759) | CRMP3, DRP-4, ULIP4 | 608407 |
ID: 127833 | synaptotagmin 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (202590596..202710454, complement) | CMS7, CMS7A, CMS7B, MYSPC, SytII | 600104 |
ID: 1808 | dihydropyrimidinase like 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (26514031..26658175) | CRMP-2, CRMP2, DHPRP2, DRP-2, DRP2, N2A3, ULIP-2, ULIP2 | 602463 |
ID: 27092 | calcium voltage-gated channel auxiliary subunit gamma 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66964707..67033398) | | 606404 |
ID: 29944 | PNMA family member 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (153056470..153060462) | MA3, MA5 | 300675 |
ID: 219409 | GS homeobox 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27792483..27794768) | GSH1, Gsh-1 | 616542 |
ID: 137970 | unc-5 netrin receptor D [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (35235475..35796540) | PRO34692, Unc5h4 | 616466 |
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: 27328 | protocadherin 11 X-linked [Homo sapiens (human)] | Chromosome X, NC_000023.11 (91779375..92623230) | PCDH-X, PCDH-Y, PCDH11, PCDH11Y, PCDH22, PCDHX, PPP1R119 | 300246 |
ID: 10687 | PNMA family member 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (26504701..26513872, complement) | MA2, MM2, RGAG2 | 603970 |
ID: 1271 | ciliary neurotrophic factor receptor [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (34551433..34590852, complement) | | 118946 |
ID: 112885 | PHD finger protein 21B [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (44881162..45010005, complement) | BHC80L, PHF4 | 616727 |