ID: 1267 | 2',3'-cyclic nucleotide 3' phosphodiesterase [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41966795..41977740) | CNP1, HLD20 | 123830 |
ID: 5238 | phosphoglucomutase 3 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (83148705..83193900, complement) | AGM1, IMD23, PAGM, PGM 3 | 172100 |
ID: 55223 | tripartite motif containing 62 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (33145399..33182043, complement) | DEAR1 | 616755 |
ID: 25793 | F-box protein 7 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (32474811..32498829) | FBX, FBX07, FBX7, PARK15, PKPS | 605648 |
ID: 1196 | CDC like kinase 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155262868..155273504, complement) | | 602989 |
ID: 3692 | eukaryotic translation initiation factor 6 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (35278906..35284772, complement) | CAB, EIF3A, ITGB4BP, b(2)gcn, eIF-6, p27(BBP), p27BBP | 602912 |
ID: 9817 | kelch like ECH associated protein 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10486125..10503356, complement) | INrf2, KLHL19 | 606016 |
ID: 140825 | neuralized E3 ubiquitin protein ligase 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45888634..45891208, complement) | C20orf163, OZZ, OZZ-E3 | 608597 |
ID: 594 | branched chain keto acid dehydrogenase E1 subunit beta [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (80106610..80466676) | BCKDE1B, BCKDH E1-beta, E1B, MSUD1B, OVD1B | 248611 |
ID: 23408 | sirtuin 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (13574274..13615158) | SIR2L5 | 604483 |
ID: 23585 | transmembrane protein 50A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (25338334..25362361) | IFNRC, SMP1 | 605348 |
ID: 57786 | RB associated KRAB zinc finger [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (5045860..5069487) | ZNF769 | 608191 |
ID: 57657 | hyperpolarization activated cyclic nucleotide gated potassium channel 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155277463..155289848) | | 609973 |
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: 84640 | ubiquitin specific peptidase 38 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (143184917..143223874) | HP43.8KD | 618322 |
ID: 7311 | ubiquitin A-52 residue ribosomal protein fusion product 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (18563766..18577550) | CEP52, HUBCEP52, L40, RPL40 | 191321 |
ID: 85359 | DiGeorge syndrome critical region gene 6 like [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (20314238..20320060, complement) | DGCR6 | 609459 |
ID: 3840 | karyopherin subunit alpha 4 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (160495007..160565571, complement) | IPOA3, QIP1, SRP3 | 602970 |
ID: 9519 | TATA-box binding protein like 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133952174..133990432) | MGC:8389, MGC:9620, STUD, TLF, TLP, TRF2 | 605521 |
ID: 23264 | zinc finger CCCH-type containing 7B [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41301525..41360147) | ROXAN1, RoXaN | 618206 |