ID: 55223 | tripartite motif containing 62 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (33145399..33182043, complement) | DEAR1 | 616755 |
ID: 2309 | forkhead box O3 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (108559825..108684774) | AF6q21, FKHRL1, FKHRL1P2, FOXO2A, FOXO3 | 602681 |
ID: 151194 | methyltransferase 21A, HSPA lysine [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (207580635..207626053, complement) | FAM119A, HCA557b, HSPA-KMT | 615257 |
ID: 4835 | N-ribosyldihydronicotinamide:quinone dehydrogenase 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (2999894..3019755) | DHQV, DIA6, NMOR2, QR2 | 160998 |
ID: 26297 | secretion regulating guanine nucleotide exchange factor [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17788048..18013047, complement) | DELGEF, Gnefr | 606051 |
ID: 23275 | protein O-fucosyltransferase 2 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (45263935..45287895, complement) | C21orf80, FUT13 | 610249 |
ID: 25793 | F-box protein 7 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (32474811..32498829) | FBX, FBX07, FBX7, PARK15, PKPS | 605648 |
ID: 2879 | glutathione peroxidase 4 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (1103994..1106779) | GPx-4, GSHPx-4, MCSP, PHGPx, SMDS, snGPx, snPHGPx | 138322 |
ID: 1196 | CDC like kinase 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155262868..155273504, complement) | | 602989 |
ID: 587 | branched chain amino acid transaminase 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (48795064..48811029, complement) | BCAM, BCATM, BCT2, HVLI, PP18 | 113530 |
ID: 515 | ATP synthase peripheral stalk-membrane subunit b [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (111449464..111462773) | ATP5F1, PIG47 | 603270 |
ID: 9817 | kelch like ECH associated protein 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10486125..10503356, complement) | INrf2, KLHL19 | 606016 |
ID: 162 | adaptor related protein complex 1 subunit beta 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29327680..29388570, complement) | ADTB1, AP105A, BAM22, CLAPB2, KIDAR | 600157 |
ID: 782 | calcium voltage-gated channel auxiliary subunit beta 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (39173453..39197669, complement) | CAB1, CACNLB1, CCHLB1 | 114207 |
ID: 85359 | DiGeorge syndrome critical region gene 6 like [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (20314238..20320060, complement) | DGCR6 | 609459 |
ID: 25851 | tectonin beta-propeller repeat containing 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (98214624..98252232, complement) | | 614781 |
ID: 282679 | aquaporin 11 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (77589953..77610356) | AQPX1 | 609914 |
ID: 27013 | cyclin Pas1/PHO80 domain containing 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (219171897..219178156, complement) | C2orf24, CGI-57 | |
ID: 55191 | NAD synthetase 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (71453203..71501816) | VCRL3 | 608285 |
ID: 30000 | transportin 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12699201..12723932, complement) | IDDHISD, IPO3, KPNB2B, TRN2 | 603002 |