ID: 146330 | F-box and leucine rich repeat protein 16 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (692500..705801, complement) | C16orf22, Fbl16, c380A1.1 | 609082 |
ID: 56896 | dihydropyrimidinase like 5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (26847995..26950351) | CRAM, CRMP-5, CRMP5, CV2, RTSC4, Ulip6 | 608383 |
ID: 27164 | spalt like transcription factor 3 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78979818..78998969) | ZNF796 | 605079 |
ID: 54734 | RAB39A, member RAS oncogene family [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107928448..107963482) | K28, RAB39 | 619558 |
ID: 222183 | serine/arginine repetitive matrix 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (76201896..76287287) | | |
ID: 1400 | collapsin response mediator protein 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (5820764..5893086, complement) | CRMP-1, DPYSL1, DRP-1, DRP1, ULIP-3 | 602462 |
ID: 2290 | forkhead box G1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (28766787..28770277) | BF1, BF2, FHKL3, FKH2, FKHL1, FKHL2, FKHL3, FKHL4A, FOXG1B, FOXG1C, HBF-1, HBF-2, HBF-3, HBF-G2, HBF2, HFK1, HFK2, HFK3, KHL2, QIN, FOXG1 | 164874 |
ID: 79948 | phospholipid phosphatase related 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (812488..823797, complement) | LPPR3, LPR3, PRG-2, PRG2 | 610391 |
ID: 29942 | purine rich element binding protein G [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (30995802..31033356, complement) | PURG-A-B, PURGA, PURGB, PURG | 618041 |
ID: 4744 | neurofilament heavy chain [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29480218..29491390) | CMT2CC, NFH | 162230 |
ID: 55871 | Zn regulated GTPase metalloprotein activator 1A [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (120837..179056, complement) | CBWD1, COBP | 611078 |
ID: 121643 | forkhead box N4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109277978..109309284, complement) | | 609429 |
ID: 140679 | solute carrier family 32 member 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38724486..38729372) | DEE114, GEFSP12, VGAT, VIAAT, VIAAT GEFSP12 | 616440 |
ID: 283576 | zinc finger DHHC-type palmitoyltransferase 22 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (77131270..77142288, complement) | C14orf59 | |
ID: 11166 | SRY-box transcription factor 21 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94709622..94712545, complement) | SOX25 | 604974 |
ID: 22983 | microtubule associated serine/threonine kinase 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12838515..12874952) | MCCCHCM, SAST | 612256 |
ID: 6585 | slit guidance ligand 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (96998038..97185959, complement) | MEGF4, SLIL1, SLIT-1, SLIT3 | 603742 |
ID: 79012 | CaM kinase like vesicle associated [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49857989..49869906, complement) | 1G5, VACAMKL | 614993 |
ID: 220107 | deleted in lymphocytic leukemia 7 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50711026..50843939, complement) | | 618634 |
ID: 94030 | leucine rich repeat containing 4B [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (50516892..50568435, complement) | HSM, LRIG4, NGL-3 | |