ID: 10956 | OS9 endoplasmic reticulum lectin [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (57694132..57721557) | ERLEC2, OS-9 | 609677 |
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: 3091 | hypoxia inducible factor 1 subunit alpha [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (61695513..61748258) | HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 | 603348 |
ID: 2099 | estrogen receptor 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (151656672..152129619) | ER, ESR, ESRA, ESTRR, Era, NR3A1 | 133430 |
ID: 672 | BRCA1 DNA repair associated [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43044295..43170327, complement) | BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4, PPP1R53, PSCP, RNF53 | 113705 |
ID: 7515 | X-ray repair cross complementing 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (43543311..43575527, complement) | RCC, SCAR26 | 194360 |
ID: 3480 | insulin like growth factor 1 receptor [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (98648539..98964530) | CD221, IGFIR, IGFR, JTK13 | 147370 |
ID: 5265 | serpin family A member 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (94376747..94390635, complement) | A1A, A1AT, AAT, PI, PI1, PRO2275, alpha1AT, nNIF | 107400 |
ID: 3309 | heat shock protein family A (Hsp70) member 5 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (125234853..125241343, complement) | BIP, GRP78, HEL-S-89n | 138120 |
ID: 846 | calcium sensing receptor [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (122183668..122291629) | CAR, EIG8, FHH, FIH, GPRC2A, HHC, HHC1, HYPOC1, NSHPT, PCAR1, hCasR | 601199 |
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: 3643 | insulin receptor [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (7112265..7294414, complement) | CD220, HHF5 | 147670 |
ID: 2305 | forkhead box M1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (2857680..2877174, complement) | FKHL16A, FOXM1B, FOXM1C, HFH-11, HFH11, HNF-3, INS-1, MPHOSPH2, MPP-2, MPP2, PIG29, TRIDENT, FOXM1 | 602341 |
ID: 4087 | SMAD family member 2 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (47808957..47930872, complement) | CHTD8, JV18, JV18-1, LDS6, MADH2, MADR2, hMAD-2, hSMAD2 | 601366 |
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: 7442 | transient receptor potential cation channel subfamily V member 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (3565446..3609411, complement) | VR1 | 602076 |
ID: 7415 | valosin containing protein [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35056064..35072625, complement) | CDC48, FTDALS6, TERA, p97 | 601023 |
ID: 7253 | thyroid stimulating hormone receptor [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80955621..81146306) | CHNG1, LGR3, hTSHR-I | 603372 |
ID: 4627 | myosin heavy chain 9 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36281280..36387967, complement) | BDPLT6, DFNA17, EPSTS, FTNS, MATINS, MHA, NMHC-II-A, NMMHC-IIA, NMMHCA | 160775 |
ID: 10855 | heparanase [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (83292461..83335153, complement) | HPA, HPA1, HPR11, HSE1, HPSE | 604724 |