ID: 259217 | heat shock protein family A (Hsp70) member 12A [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (116671192..116850747, complement) | | 610701 |
ID: 55323 | La ribonucleoprotein 6, translational regulator [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (70829130..70854157, complement) | ACHN | 611300 |
ID: 7004 | TEA domain transcription factor 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (2959397..3040676) | EFTR-2, RTEF1, TCF13L1, TEF-3, TEF3, TEFR-1, hRTEF-1B | 601714 |
ID: 5217 | profilin 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (149964904..149970895, complement) | D3S1319E, PFL | 176590 |
ID: 22808 | muscle RAS oncogene homolog [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (138347648..138405535) | M-RAs, NS11, R-RAS3, RRAS3 | 608435 |
ID: 144165 | prickle planar cell polarity protein 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (42456757..42589746, complement) | EPM1B, RILP | 608500 |
ID: 140735 | dynein light chain LC8-type 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (58083419..58095542) | DNCL1B, Dlc2, RSPH22 | 608942 |
ID: 23516 | solute carrier family 39 member 14 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22367278..22434129) | HCIN, HMNDYT2, LZT-Hs4, NET34, ZIP14, cig19 | 608736 |
ID: 2817 | glypican 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (240435663..240468076) | glypican | 600395 |
ID: 8671 | solute carrier family 4 member 4 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (71062660..71572083) | HNBC1, KNBC, NBC1, NBC2, NBCe1, NBCe1-A, PRTAO, SLC4A5, hhNMC, kNBC1, pNBC | 603345 |
ID: 64359 | nucleoredoxin [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (799310..979776, complement) | NRX, RRS2, TRG-4 | 612895 |
ID: 84617 | tubulin beta 6 class V [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (12307669..12329826) | FPVEPD, HsT1601, TUBB-5 | 615103 |
ID: 3614 | inosine monophosphate dehydrogenase 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128392277..128409982, complement) | IMPD, IMPD1, IMPDH-I, LCA11, RP10, sWSS2608 | 146690 |
ID: 83604 | transmembrane protein 47 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (34627075..34657285, complement) | BCMP1, TM4SF10, VAB-9 | 300698 |
ID: 2195 | FAT atypical cadherin 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (186587794..186726696, complement) | CDHF7, CDHR8, FAT, ME5, hFat1 | 600976 |
ID: 23001 | WD repeat and FYVE domain containing 3 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (84669597..84966690, complement) | ALFY, BCHS, MCPH18, ZFYVE25 | 617485 |
ID: 9282 | mediator complex subunit 14 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (40648305..40736159, complement) | CRSP150, CRSP2, CSRP, CXorf4, DRIP150, EXLM1, RGR1, TRAP170 | 300182 |
ID: 2743 | glycine receptor beta [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (157076150..157172090) | HKPX2 | 138492 |
ID: 23158 | TBC1 domain family member 9 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (140620782..140756385, complement) | GRAMD9, MDR1 | 618035 |
ID: 51429 | sorting nexin 9 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (157823246..157945077) | SDP1, SH3PX1, SH3PXD3A, WISP | 605952 |