ID: 79007 | dysbindin domain containing 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (90004871..90019890, complement) | | 620388 |
ID: 124997 | WD repeat domain 81 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (1716523..1738585) | CAMRQ2, CHMRQ, HYC3, PPP1R166, SORF-2 | 614218 |
ID: 114879 | oxysterol binding protein like 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (3087107..3165310, complement) | OBPH1, ORP5 | 606733 |
ID: 2050 | EPH receptor B4 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (100802565..100827523, complement) | CMAVM2, HFASD, HTK, LMPHM7, MYK1, TYRO11 | 600011 |
ID: 64324 | nuclear receptor binding SET domain protein 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (177131798..177300213) | ARA267, KMT3B, SOTOS, SOTOS1, STO | 606681 |
ID: 115207 | potassium channel tetramerization domain containing 12 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (76880175..76886405, complement) | C13orf2, PFET1, PFETIN | 610521 |
ID: 6452 | SH3 domain binding protein 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (2793085..2841096) | 3BP-2, 3BP2, CRBM, CRPM, RES4-23 | 602104 |
ID: 5527 | protein phosphatase 2 regulatory subunit B'gamma [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (101760573..101927992) | B56G, B56gamma, PR61G | 601645 |
ID: 112398 | egl-9 family hypoxia inducible factor 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40799191..40808434) | EIT-6, EIT6, HIF-PH1, HIFPH1, HPH-1, HPH-3, PHD1 | 606424 |
ID: 26088 | golgi associated, gamma adaptin ear containing, ARF binding protein 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37608834..37633564) | | 606004 |
ID: 80318 | G kinase anchoring protein 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83739425..83817769, complement) | FKSG21, GKAP42 | 611356 |
ID: 8454 | cullin 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (148697756..148801110) | | 603134 |
ID: 60436 | TGFB induced factor homeobox 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (36573464..36593950) | | 607294 |
ID: 158405 | KIAA1958 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (112486827..112669397) | | 617390 |
ID: 2152 | coagulation factor III, tissue factor [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (94529173..94541759, complement) | CD142, TF, TFA | 134390 |
ID: 6397 | SEC14 like lipid binding 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (77088685..77217101) | PRELID4A, SEC14L | 601504 |
ID: 91300 | R3H domain containing 4 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (896503..913219, complement) | C19orf22 | |
ID: 10518 | calcium and integrin binding family member 2 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (78104606..78131535, complement) | DFNB48, KIP2, USH1J | 605564 |
ID: 80148 | solute carrier family 66 member 2 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79902420..79951653, complement) | PQLC1 | |
ID: 22893 | bromo adjacent homology domain containing 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (40437452..40468236) | | 613880 |