ID: 57338 | junctophilin 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87601835..87698156) | CAGL237, HDL2, JP-3, JP3, TNRC22 | 605268 |
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: 4852 | neuropeptide Y [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (24284190..24291862) | PYY4 | 162640 |
ID: 56896 | dihydropyrimidinase like 5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (26847995..26950351) | CRAM, CRMP-5, CRMP5, CV2, RTSC4, Ulip6 | 608383 |
ID: 5459 | POU class 4 homeobox 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (146338839..146341728) | BRN3C, DFNA15, DFNA42, DFNA52 | 602460 |
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: 55871 | Zn regulated GTPase metalloprotein activator 1A [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (120837..179056, complement) | CBWD1, COBP | 611078 |
ID: 220107 | deleted in lymphocytic leukemia 7 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50711026..50843939, complement) | | 618634 |
ID: 56936 | coiled-coil domain containing 177 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (69569799..69574871, complement) | C14orf162, PLPL | |
ID: 79948 | phospholipid phosphatase related 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (812488..823797, complement) | LPPR3, LPR3, PRG-2, PRG2 | 610391 |
ID: 7067 | thyroid hormone receptor alpha [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (40062193..40093867) | AR7, CHNG6, EAR7, ERB-T-1, ERBA, ERBA1, NR1A11, THRA2, THRalpha, THRalpha1, THRalpha2, TRalpha, TRalpha1, TRalpha2, c-ERBA-1, c-erbA, THRA | 190120 |
ID: 4062 | lymphocyte antigen 6 family member H [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143157916..143160654, complement) | NMLY6 | 603625 |
ID: 4829 | neuromedin B receptor [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (142074484..142147122, complement) | BB1, BB1R, BRS1, NMB-R | 162341 |
ID: 6656 | SRY-box transcription factor 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (112067149..112071706) | | 602148 |
ID: 222183 | serine/arginine repetitive matrix 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (76201896..76287287) | | |
ID: 375607 | N-acetyltransferase 16 (putative) [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101170496..101180293, complement) | C7orf52 | 615783 |
ID: 4761 | neuronal differentiation 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (39603768..39607920, complement) | DEE72, EIEE72, NDRF, bHLHa1 | 601725 |
ID: 10472 | zinc finger and BTB domain containing 18 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (244048491..244057476) | C1DELq42q44, C1DELq43q44, C2H2-171, DEL1Q42Q44, DEL1Q43Q44, MRD22, RP58, TAZ-1, ZNF238 | 608433 |
ID: 146330 | F-box and leucine rich repeat protein 16 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (692500..705801, complement) | C16orf22, Fbl16, c380A1.1 | 609082 |
ID: 343702 | XK related 7 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (31968151..32003387) | C20orf159, dJ310O13.4 | |