ID: 1002 | cadherin 4 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (61252261..61940617) | CAD4, R-CAD, RCAD | 603006 |
ID: 2676 | GDNF family receptor alpha 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (138252380..138274621, complement) | GDNFR3 | 605710 |
ID: 10227 | major facilitator superfamily domain containing 10 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (2930567..2934825, complement) | TETRAN, TETTRAN | 610977 |
ID: 78999 | leucine rich repeat and fibronectin type III domain containing 4 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66857064..66860475) | FIGLER6, SALM3, SALM3. | 612810 |
ID: 576 | adhesion G protein-coupled receptor B2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (31727117..31764340, complement) | BAI2 | 602683 |
ID: 284338 | proline rich 19 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (42302132..42310814) | | |
ID: 23603 | coronin 1C [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (108645109..108731518, complement) | HCRNN4 | 605269 |
ID: 5600 | mitogen-activated protein kinase 11 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (50263713..50270380, complement) | P38B, P38BETA2, PRKM11, SAPK2, SAPK2B, p38-2, p38Beta | 602898 |
ID: 64864 | regulatory factor X7 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (56087280..56245082, complement) | MRD71, RFXDC2 | 612660 |
ID: 92312 | mex-3 RNA binding family member A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156072013..156082465, complement) | MEX-3A, RKHD4, RNF162 | 611007 |
ID: 23380 | SLIT-ROBO Rho GTPase activating protein 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (206203541..206464436) | ARHGAP34, FNBP2A, SRGAP3, SRGAP2 | 606524 |
ID: 374654 | kinesin family member 7 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (89617309..89663049, complement) | ACLS, AGBK, HLS2, JBTS12, MMEDF, UNQ340 | 611254 |
ID: 3925 | stathmin 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (25884179..25906880, complement) | C1orf215, LAP18, Lag, OP18, PP17, PP19, PR22, SMN | 151442 |
ID: 6608 | smoothened, frizzled class receptor [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (129188633..129213545) | CRJS, FZD11, Gx, PHLSH, SMO | 601500 |
ID: 388677 | notch 2 N-terminal like A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (146148865..146229021, complement) | N2N, NOTCH2NL | 618023 |
ID: 222865 | transmembrane protein 130 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (98846490..98870014, complement) | | |
ID: 1949 | ephrin B3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7705202..7711372) | EFL6, EPLG8, LERK8 | 602297 |
ID: 10391 | coronin 2B [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (68518373..68727806) | CLIPINC | 605002 |
ID: 163033 | zinc finger protein 579 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (55576774..55580848, complement) | | |
ID: 80757 | transmembrane protein 121 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (105526583..105530198) | TMEM121A, hhole, hole | |