ID: 6687 | SPG7 matrix AAA peptidase subunit, paraplegin [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89508388..89557768) | CAR, CMAR, PGN, SPG5C | 602783 |
ID: 7852 | C-X-C motif chemokine receptor 4 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (136114349..136118149, complement) | CD184, D2S201E, FB22, HM89, HSY3RR, LAP-3, LAP3, LCR1, LESTR, NPY3R, NPYR, NPYRL, NPYY3R, WHIM, WHIMS, WHIMS1 | 162643 |
ID: 2100 | estrogen receptor 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64226707..64338613, complement) | ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2, ODG8 | 601663 |
ID: 6513 | solute carrier family 2 member 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (42925353..42958868, complement) | CSE, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT-1, GLUT1, GLUT1DS, HTLVR, PED, SDCHCN | 138140 |
ID: 682 | basigin (Ok blood group) [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (571283..583493) | 5F7, CD147, EMMPRIN, EMPRIN, HAb18G, OK, TCSF | 109480 |
ID: 3117 | major histocompatibility complex, class II, DQ alpha 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32637406..32655272) | CELIAC1, DQ-A1, DQA1, HLA-DQA*, HLA-DQB1, HLA-DQA1 | 146880 |
ID: 23586 | RNA sensor RIG-I [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (32455302..32526196, complement) | DDX58, RIG-I, RIG1, RLR-1, SGMRT2 | 609631 |
ID: 2214 | Fc gamma receptor IIIa [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (161541759..161550737, complement) | CD16, CD16-II, CD16A, FCG3, FCGR3, FCGRIII, FCR-10, FCRIII, FCRIIIA, FcGRIIIA, IGFR3, IMD20 | 146740 |
ID: 10155 | tripartite motif containing 28 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (58544064..58550715) | KAP1, PPP1R157, RNF96, TF1B, TIF1B, TIF1beta | 601742 |
ID: 5727 | patched 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95442980..95516971, complement) | BCNS, BCNS1, NBCCS, PTC, PTC1, PTCH | 601309 |
ID: 773 | calcium voltage-gated channel subunit alpha1 A [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (13206442..13506479, complement) | APCA, BI, CACNL1A4, CAV2.1, DEE42, EA2, EIEE42, FHM, HPCA, MHP, MHP1, SCA6 | 601011 |
ID: 3190 | heterogeneous nuclear ribonucleoprotein K [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83968083..83980615, complement) | AUKS, CSBP, HNRPK, TUNP | 600712 |
ID: 624 | bradykinin receptor B2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96204839..96244164) | B2R, BK-2, BK2, BKR2, BRB2 | 113503 |
ID: 360 | aquaporin 3 (Gill blood group) [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (33441160..33447593, complement) | AQP-3, GIL | 600170 |
ID: 6517 | solute carrier family 2 member 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7281718..7288257) | GLUT4 | 138190 |
ID: 9290 | G protein-coupled receptor 55 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (230907328..230961201, complement) | LPIR1 | 604107 |
ID: 407009 | microRNA 224 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (151958578..151958658, complement) | MIRN224, miRNA224 | 300769 |
ID: 6770 | steroidogenic acute regulatory protein [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (38142700..38150952, complement) | STARD1 | 600617 |
ID: 6428 | serine and arginine rich splicing factor 3 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (36594362..36605600) | SFRS3, SRp20 | 603364 |
ID: 10197 | proteasome activator subunit 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42833397..42843760) | HEL-S-283, Ki, PA28-gamma, PA28G, PA28gamma, REG-GAMMA | 605129 |