ID: 84952 | cingulin like 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (57376505..57550717) | JACOP, PCING | 607856 |
ID: 59277 | netrin 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95657807..95791155, complement) | PRO3091 | 610401 |
ID: 55556 | enolase superfamily member 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (662986..712630, complement) | FUCD, RTS, TYMSAS | 607427 |
ID: 23286 | WW and C2 domain containing 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (168291645..168472303) | HBEBP3, HBEBP36, KIBRA, MEMRYQTL, PPP1R168 | 610533 |
ID: 126969 | solute carrier family 44 member 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (94820357..94895247) | CTL3 | 620328 |
ID: 283638 | centrosomal protein 170B [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (104864513..104896747) | CEP170R, FAM68C, KIAA0284 | 620251 |
ID: 114569 | mal, T cell differentiation protein 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (119208363..119245673) | | 609684 |
ID: 26033 | attractin like 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (115093365..115948999) | ALP, bA338L11.1, bA454H24.1 | 612869 |
ID: 2260 | fibroblast growth factor receptor 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (38411143..38468635, complement) | BFGFR, CD331, CEK, ECCL, FGFBR, FGFR-1, FLG, FLT-2, FLT2, HBGFR, HH2, HRTFDS, KAL2, N-SAM, OGD, bFGF-R-1 | 136350 |
ID: 154807 | vitamin K epoxide reductase complex subunit 1 like 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (65865772..65959558) | | 608838 |
ID: 1981 | eukaryotic translation initiation factor 4 gamma 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (184314606..184335358) | EIF-4G1, EIF4F, EIF4G, EIF4GI, P220, PARK18 | 600495 |
ID: 2619 | growth arrest specific 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86944362..86947506, complement) | | 139185 |
ID: 5727 | patched 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95442980..95516971, complement) | BCNS, BCNS1, NBCCS, PTC, PTC1, PTCH | 601309 |