ID: 113277 | transmembrane protein 106A [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43211875..43220041) | | |
ID: 1956 | epidermal growth factor receptor [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (55019017..55211628) | ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS, PIG61, mENA | 131550 |
ID: 351 | amyloid beta precursor protein [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (25880550..26171128, complement) | AAA, ABETA, ABPP, AD1I, CTFgamma, CVAP, PN-II, PN2, alpha-sAPP, preA4, APP | 104760 |
ID: 3123 | major histocompatibility complex, class II, DR beta 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32578775..32589848, complement) | DRB1, HLA-DR1B, HLA-DRB, SS1 | 142857 |
ID: 3162 | heme oxygenase 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (35381096..35394207) | HMOX1D, HO-1, HSP32, bK286B10 | 141250 |
ID: 3119 | major histocompatibility complex, class II, DQ beta 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32659467..32666657, complement) | CELIAC1, HLA-DQB, IDDM1 | 604305 |
ID: 3077 | homeostatic iron regulator [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (26087429..26098343) | HFE1, HH, HLA-H, MVCD7, TFQTL2 | 613609 |
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: 3949 | low density lipoprotein receptor [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (11089463..11133820) | FH, FHC, FHCL1, LDLCQ2 | 606945 |
ID: 9518 | growth differentiation factor 15 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (18386158..18389176) | GDF-15, HG, MIC-1, MIC1, NAG-1, PDF, PLAB, PTGFB | 605312 |
ID: 3643 | insulin receptor [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (7112265..7294414, complement) | CD220, HHF5 | 147670 |
ID: 100874261 | coiled-coil domain containing 200 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43221417..43231269, complement) | LINC00854, TMEM106A-AS1 | |
ID: 3685 | integrin subunit alpha V [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (186590056..186680901) | CD51, MSK8, VNRA, VTNR | 193210 |
ID: 6786 | stromal interaction molecule 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (3854604..4093210) | D11S4896E, GOK, IMD10, STRMK, TAM, TAM1 | 605921 |
ID: 6868 | ADAM metallopeptidase domain 17 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (9488486..9555830, complement) | ADAM18, CD156B, CSVP, NISBD, NISBD1, TACE | 603639 |
ID: 3678 | integrin subunit alpha 5 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (54395261..54419266, complement) | CD49e, FNRA, VLA-5, VLA5A | 135620 |
ID: 102 | ADAM metallopeptidase domain 10 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (58588809..58749707, complement) | AD10, AD18, CD156c, CDw156, HsT18717, MADM, RAK, kuz | 602192 |
ID: 2159 | coagulation factor X [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113122799..113149529) | FX, FXA | 613872 |
ID: 4907 | 5'-nucleotidase ecto [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (85450083..85495784) | CALJA, CD73, E5NT, NT, NT5, NTE, eN, eNT | 129190 |
ID: 3133 | major histocompatibility complex, class I, E [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30489509..30494194) | HLA-6.2, QA1 | 143010 |