| ID: 158062 | lipocalin 6 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136744017..136748525, complement) | LCN5, UNQ643, hLcn5 | 609379 |
| ID: 6714 | SRC proto-oncogene, non-receptor tyrosine kinase [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (37344699..37406050) | ASV1, THC6, c-SRC, p60-Src, SRC | 190090 |
| ID: 3309 | heat shock protein family A (Hsp70) member 5 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (125234853..125241343, complement) | BIP, GRP78, HEL-S-89n | 138120 |
| ID: 7474 | Wnt family member 5A [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (55465715..55505263, complement) | hWNT5A | 164975 |
| ID: 590 | butyrylcholinesterase [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (165772904..165837423, complement) | BCHED, CHE1, CHE2, E1 | 177400 |
| ID: 5167 | ectonucleotide pyrophosphatase/phosphodiesterase 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (131808020..131895155) | ARHR2, COLED, M6S1, NPP1, NPPS, PC-1, PCA1, PDNP1 | 173335 |
| ID: 655 | bone morphogenetic protein 7 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (57168753..57266641, complement) | OP-1 | 112267 |
| ID: 3676 | integrin subunit alpha 4 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (181457205..181538940) | CD49D, IA4 | 192975 |
| ID: 5360 | phospholipid transfer protein [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45898620..45912155, complement) | BPIFE, HDLCQ9 | 172425 |
| ID: 10507 | semaphorin 4D [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (89360787..89498113, complement) | A8, BB18, C9orf164, CD100, COLL4, GR3, M-sema-G, SEMAJ, coll-4 | 601866 |
| ID: 2182 | acyl-CoA synthetase long chain family member 4 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (109641335..109733257, complement) | ACS4, FACL4, LACS4, MRX63, MRX68, XLID63 | 300157 |
| ID: 23765 | interleukin 17 receptor A [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (17085000..17115693) | CANDF5, CD217, CDw217, IL-17RA, IL17R, IMD51, hIL-17R | 605461 |
| ID: 3425 | alpha-L-iduronidase [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (986997..1008351) | IDA, MPS1, MPSI | 252800 |
| ID: 5270 | serpin family E member 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (223975045..224039286, complement) | GDN, GDNPF, PI-7, PI7, PN-1, PN1, PNI | 177010 |
| ID: 1690 | cochlin [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (30874559..30895615) | COCH-5B25B2, DFNA9, DFNB110, COCH | 603196 |
| ID: 649 | bone morphogenetic protein 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22165372..22212326) | OI13, PCOLC, PCP, PCP2, TLD | 112264 |
| ID: 411 | arylsulfatase B [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (78777209..78985958, complement) | ASB, G4S, MPS6 | 611542 |
| ID: 10220 | growth differentiation factor 11 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (55743122..55757264) | BMP-11, BMP11, VHO | 603936 |
| ID: 55959 | sulfatase 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (47657406..47786627, complement) | HSULF-2 | 610013 |
| ID: 7358 | UDP-glucose 6-dehydrogenase [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (39498755..39527439, complement) | DEE84, EIEE84, GDH, UDP-GlcDH, UDPGDH, UGD | 603370 |