ID: 6570 | solute carrier family 18 member A1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (20144855..20183136, complement) | CGAT, VAT1, VMAT1 | 193002 |
ID: 29126 | CD274 molecule [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (5450542..5470554) | B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1, PDL1, hPD-L1 | 605402 |
ID: 5133 | programmed cell death 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241849884..241858894, complement) | AIMTBS, CD279, PD-1, PD1, SLEB2, hPD-1, hPD-l, hSLE1 | 600244 |
ID: 2706 | gap junction protein beta 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20187470..20192938, complement) | BAPS, CX26, DFNA3, DFNA3A, DFNB1, DFNB1A, HID, KID, NSRD1, PPK | 121011 |
ID: 338 | apolipoprotein B [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (21001429..21044073, complement) | FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48 | 107730 |
ID: 3107 | major histocompatibility complex, class I, C [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31268749..31272092, complement) | D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1 | 142840 |
ID: 10018 | BCL2 like 11 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (111120914..111168445) | BAM, BIM, BOD | 603827 |
ID: 7037 | transferrin receptor [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196049284..196082090, complement) | CD71, IMD46, T9, TFR, TFR1, TR, TRFR, p90 | 190010 |
ID: 5376 | peripheral myelin protein 22 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (15229779..15265326, complement) | CIDP, CMT1A, CMT1E, DSS, GAS-3, GAS3, HMSNIA, HNPP, Sp110 | 601097 |
ID: 975 | CD81 molecule [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2376180..2397397) | CVID6, S5.7, TAPA1, TSPAN28 | 186845 |
ID: 5354 | proteolipid protein 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (103776506..103792619) | GPM6C, HLD1, MMPL, PLP, PLP/DM20, PMD, SPG2 | 300401 |
ID: 6319 | stearoyl-CoA desaturase [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (100347233..100364826) | FADS5, MSTP0081, SCDOS, hSCD1, SCD | 604031 |
ID: 169026 | solute carrier family 30 member 8 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (116950217..117176714) | ZNT8, ZnT-8 | 611145 |
ID: 100506658 | occludin [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (69492547..69558104) | BLCPMG, PPP1R115, PTORCH1 | 602876 |
ID: 1287 | collagen type IV alpha 5 chain [Homo sapiens (human)] | Chromosome X, NC_000023.11 (108439838..108697545) | ASLN, ATS, ATS1, CA54 | 303630 |
ID: 58191 | C-X-C motif chemokine ligand 16 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (4733533..4739928, complement) | CXCLG16, SR-PSOX, SRPSOX | 605398 |
ID: 3992 | fatty acid desaturase 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (61799627..61817003, complement) | D5D, FADS6, FADSD5, LLCDL1, TU12 | 606148 |
ID: 51094 | adiponectin receptor 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (202940825..202958572, complement) | ACDCR1, CGI-45, CGI45, PAQR1, TESBP1A | 607945 |
ID: 2030 | solute carrier family 29 member 1 (Augustine blood group) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (44219615..44234142) | AUG, ENT1, hENT1 | 602193 |
ID: 931 | membrane spanning 4-domains A1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (60455847..60470752) | B1, Bp35, CD20, CVID5, FMC7, LEU-16, S7 | 112210 |