ID: 117145 | thioesterase superfamily member 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151870866..151909511, complement) | CTMP | 606388 |
ID: 207 | AKT serine/threonine kinase 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (104769349..104795748, complement) | AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA | 164730 |
ID: 857 | caveolin 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (116525009..116561185) | BSCL3, CGL3, LCCNS, MSTP085, PPH3, VIP21 | 601047 |
ID: 4869 | nucleophosmin 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (171387116..171410900) | B23, NPM | 164040 |
ID: 11315 | Parkinsonism associated deglycase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (7961711..7985505) | DJ-1, DJ1, GATD2, HEL-S-67p | 602533 |
ID: 3329 | heat shock protein family D (Hsp60) member 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (197486584..197500274, complement) | CPN60, GROEL, HLD4, HSP-60, HSP60, HSP65, HuCHA60, SPG13 | 118190 |
ID: 7345 | ubiquitin C-terminal hydrolase L1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (41256928..41268455) | HEL-117, HEL-S-53, NDGOA, PARK5, PGP 9.5, PGP9.5, PGP95, SPG79, SPG79A, UCHL-1, Uch-L1 | 191342 |
ID: 5443 | proopiomelanocortin [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (25160860..25168580, complement) | ACTH, CLIP, LPH, MSH, NPP, OBAIRH, POC | 176830 |
ID: 7019 | transcription factor A, mitochondrial [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (58385410..58399220) | MTDPS15, MTTF1, MTTFA, TCF6, TCF6L1, TCF6L2, TCF6L3 | 600438 |
ID: 572 | BCL2 associated agonist of cell death [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (64269828..64284704, complement) | BBC2, BCL2L8 | 603167 |
ID: 27113 | BCL2 binding component 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47220824..47232860, complement) | JFY-1, JFY1, PUMA | 605854 |
ID: 708 | complement C1q binding protein [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (5432777..5439155, complement) | COXPD33, GC1QBP, HABP1, SF2AP32, SF2p32, gC1Q-R, gC1qR, p32 | 601269 |
ID: 10131 | TNF receptor associated protein 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (3658037..3717524, complement) | HSP 75, HSP75, HSP90L, TRAP-1 | 606219 |
ID: 5160 | pyruvate dehydrogenase E1 subunit alpha 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (19343927..19361718) | E1alpha, PDHA, PDHAD, PDHCE1A, PHE1A | 300502 |
ID: 3191 | heterogeneous nuclear ribonucleoprotein L [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (38836370..38852347, complement) | HNRPL, P/OKcl.14, hnRNP-L | 603083 |
ID: 9361 | lon peptidase 1, mitochondrial [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (5691834..5720452, complement) | CODASS, LON, LONP, LonHS, PIM1, PRSS15, hLON | 605490 |
ID: 5163 | pyruvate dehydrogenase kinase 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (172555373..172724312) | | 602524 |
ID: 64170 | caspase recruitment domain family member 9 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136363956..136373669, complement) | CANDF2, IMD103, hCARD9 | 607212 |
ID: 23408 | sirtuin 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (13574274..13615158) | SIR2L5 | 604483 |
ID: 10128 | leucine rich pentatricopeptide repeat containing [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (43886224..43996265, complement) | CLONE-23970, GP130, LRP130, LSFC, MC4DN5 | 607544 |