ID: 140679 | solute carrier family 32 member 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38724486..38729372) | DEE114, GEFSP12, VGAT, VIAAT, VIAAT GEFSP12 | 616440 |
ID: 4062 | lymphocyte antigen 6 family member H [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143157916..143160654, complement) | NMLY6 | 603625 |
ID: 3780 | potassium calcium-activated channel subfamily N member 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17951290..18000085) | KCa2.1, SK1, SKCA1, hSK1 | 602982 |
ID: 1400 | collapsin response mediator protein 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (5820764..5893086, complement) | CRMP-1, DPYSL1, DRP-1, DRP1, ULIP-3 | 602462 |
ID: 222183 | serine/arginine repetitive matrix 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (76201896..76287287) | | |
ID: 56896 | dihydropyrimidinase like 5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (26847995..26950351) | CRAM, CRMP-5, CRMP5, CV2, RTSC4, Ulip6 | 608383 |
ID: 6656 | SRY-box transcription factor 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (112067149..112071706) | | 602148 |
ID: 10814 | complexin 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (175796533..175884021) | 921-L, CPX-2, CPX2, Hfb1 | 605033 |
ID: 128414 | sodium/potassium transporting ATPase interacting 4 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63240784..63254921, complement) | C20orf58, FAM77A, bA261N11.2 | 612873 |
ID: 124274 | G protein-coupled receptor 139 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20028239..20073890, complement) | GPRg1, PGR3 | 618448 |
ID: 375607 | N-acetyltransferase 16 (putative) [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101170496..101180293, complement) | C7orf52 | 615783 |
ID: 85300 | ATCAY kinesin light chain interacting caytaxin [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (3880685..3928082) | BNIP-H, CLAC | 608179 |
ID: 1995 | ELAV like RNA binding protein 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (11451326..11481046, complement) | HUC, HUCL, PLE21 | 603458 |
ID: 83723 | TLC domain containing 3B [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30024427..30053040, complement) | CORD22, FAM57B, FP1188 | 615175 |
ID: 56936 | coiled-coil domain containing 177 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (69569799..69574871, complement) | C14orf162, PLPL | |
ID: 94030 | leucine rich repeat containing 4B [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (50516892..50568435, complement) | HSM, LRIG4, NGL-3 | |
ID: 57648 | NHS like 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (32741830..32774970) | KIAA1522 | |
ID: 5459 | POU class 4 homeobox 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (146338839..146341728) | BRN3C, DFNA15, DFNA42, DFNA52 | 602460 |
ID: 4761 | neuronal differentiation 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (39603768..39607920, complement) | DEE72, EIEE72, NDRF, bHLHa1 | 601725 |
ID: 1463 | neurocan [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (19211958..19252233) | CSPG3 | 600826 |