ID: 10058 | ATP binding cassette subfamily B member 6 (LAN blood group) [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (219209772..219218958, complement) | ABC, LAN, MTABC3, PRP, umat | 605452 |
ID: 7124 | tumor necrosis factor [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31575565..31578336) | DIF, IMD127-alpha, TNFA, TNFSF2, TNLG1F, TNF | 191160 |
ID: 2099 | estrogen receptor 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (151656672..152129619) | ER, ESR, ESRA, ESTRR, Era, NR3A1 | 133430 |
ID: 5243 | ATP binding cassette subfamily B member 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (87503017..87713295, complement) | ABC20, CD243, CLCS, ENPAT, GP170, MDR1, P-GP, PGY1, p-170 | 171050 |
ID: 3106 | major histocompatibility complex, class I, B [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31353875..31357179, complement) | AS, B-4901, HLAB | 142830 |
ID: 9429 | ATP binding cassette subfamily G member 2 (JR blood group) [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (88090264..88231626, complement) | ABC15, ABCP, BCRP, BCRP1, BMDP, CD338, CDw338, CDw388, EST157481, GOUT1, MRX, MXR, MXR-1, MXR1, UAQTL1 | 603756 |
ID: 196 | aryl hydrocarbon receptor [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (17298652..17346147) | FVH3, RP85, bHLHe76 | 600253 |
ID: 2896 | granulin precursor [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44345302..44353106) | CLN11, FTD2, GEP, GP88, PCDGF, PEPI, PGRN | 138945 |
ID: 648 | BMI1 proto-oncogene, polycomb ring finger [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (22321099..22331706) | FLVI2/BMI1, PCGF4, RNF51, flvi-2/bmi-1 | 164831 |
ID: 6833 | ATP binding cassette subfamily C member 8 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17392498..17476845, complement) | ABC36, HHF1, HI, HRINS, MRP8, PHHI, PNDM3, SUR, SUR1, SUR1delta2, TNDM2 | 600509 |
ID: 4162 | melanoma cell adhesion molecule [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (119308529..119317130, complement) | CD146, HEMCAM, METCAM, MUC18, MelCAM | 155735 |
ID: 2177 | FA complementation group D2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (10026437..10101932) | FA-D2, FA4, FACD, FAD, FAD2, FANCD | 613984 |
ID: 4864 | NPC intracellular cholesterol transporter 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (23506184..23586506, complement) | NPC, POGZ, SLC65A1 | 607623 |
ID: 9619 | ATP binding cassette subfamily G member 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42199689..42297244) | ABC8, WHITE1 | 603076 |
ID: 214 | activated leukocyte cell adhesion molecule [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (105366909..105576900) | CD166, MEMD | 601662 |
ID: 6510 | solute carrier family 1 member 5 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46774883..46788594, complement) | AAAT, ASCT2, ATBO, M7V1, M7VS1, R16, RDRC | 109190 |
ID: 10456 | HCLS1 associated protein X-1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (154272629..154275875) | HCLSBP1, HS1BP1, SCN3 | 605998 |
ID: 10452 | translocase of outer mitochondrial membrane 40 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (44891254..44903689) | C19orf1, D19S1177E, PER-EC1, PEREC1, TOM40 | 608061 |
ID: 2771 | G protein subunit alpha i2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (50227068..50263358) | GIPB, HG1C, H_LUCA15.1, H_LUCA16.1, GNAI2 | 139360 |
ID: 3113 | major histocompatibility complex, class II, DP alpha 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (33064569..33080748, complement) | DP(W3), DP(W4), DPA1, HLA-DP1A, HLA-DPA, HLA-DPB1, HLADP, HLASB, PLT1 | 142880 |