ID: 11332 | acyl-CoA thioesterase 7 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6264272..6393767, complement) | ACH1, ACT, BACH, CTE-II, LACH, LACH1, hBACH | 602587 |
ID: 64840 | porcupine O-acyltransferase [Homo sapiens (human)] | Chromosome X, NC_000023.11 (48508992..48520814) | DHOF, FODH, MG61, PORC, PPN | 300651 |
ID: 8611 | phospholipid phosphatase 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (55424854..55534964, complement) | LLP1a, LPP1, PAP-2a, PAP2, PPAP2A | 607124 |
ID: 3589 | interleukin 11 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (55364382..55370463, complement) | AGIF, IL-11 | 147681 |
ID: 54677 | carnitine O-octanoyltransferase [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (87345664..87399794) | COT | 606090 |
ID: 133957 | coiled-coil domain containing 127 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (196868..218153, complement) | | |
ID: 54825 | cadherin related family member 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (176542511..176595974) | PCDH24, PCLCK, PCLKC | 619713 |
ID: 388962 | bolA family member 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (74135400..74147912, complement) | MMDS2 | 613183 |
ID: 79078 | chromosome 1 open reading frame 50 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (42767249..42779491) | | |
ID: 85359 | DiGeorge syndrome critical region gene 6 like [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (20314238..20320060, complement) | DGCR6 | 609459 |
ID: 85302 | Fas binding factor 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (75909574..75941042, complement) | Alb, FBF-1 | 616807 |
ID: 55752 | septin 11 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (76949752..77040154) | SEPT11, Septin-11 | 612887 |
ID: 706 | translocator protein [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43151559..43163242) | BPBS, BZRP, DBI, IBP, MBR, PBR, PBS, PKBS, PTBR1, mDRC, pk18, TSPO | 109610 |
ID: 10539 | glutaredoxin 3 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (130136391..130180377) | GLRX4, GRX3, GRX4, PICOT, TXNL2, TXNL3 | 612754 |
ID: 10054 | ubiquitin like modifier activating enzyme 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34428381..34471251) | ACCES, ARX, HRIHFB2115, SAE2 | 613295 |
ID: 25793 | F-box protein 7 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (32474811..32498829) | FBX, FBX07, FBX7, PARK15, PKPS | 605648 |
ID: 6415 | selenoprotein W [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47778703..47784682) | SEPW1, selW | 603235 |
ID: 25813 | SAMM50 sorting and assembly machinery component [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (43955442..43996529) | CGI-51, OMP85, SAM50, TOB55, TRG-3, YNL026W | 612058 |
ID: 112611 | RWD domain containing 2A [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (83193357..83198935) | RWDD2, dJ747H23.2 | |
ID: 51667 | negative regulator of ubiquitin like proteins 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (151341812..151378449) | BS4L, NYREN18, NUB1 | 607981 |