ID: 8646 | chordin [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (184380054..184390739) | | 603475 |
ID: 9370 | adiponectin, C1Q and collagen domain containing [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (186842710..186858463) | ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1, GBP28 | 605441 |
ID: 4088 | SMAD family member 3 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (67065602..67195169) | HSPC193, HsT17436, JV15-2, LDS1C, LDS3, MADH3, hMAD-3, hSMAD3, mad3 | 603109 |
ID: 650 | bone morphogenetic protein 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (6767686..6780246) | BDA2A, SSFSC, SSFSC1, BMP2 | 112261 |
ID: 652 | bone morphogenetic protein 4 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (53949736..53956891, complement) | BMP2B, BMP2B1, MCOPS6, OFC11, ZYME | 112262 |
ID: 948 | CD36 molecule (CD36 blood group) [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (80602207..80679274) | BDPLT10, CHDS7, FAT, GP3B, GP4, GPIV, PASIV, SCARB3 | 173510 |
ID: 5156 | platelet derived growth factor receptor alpha [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (54229293..54298245) | CD140A, PDGFR-2, PDGFR2 | 173490 |
ID: 2149 | coagulation factor II thrombin receptor [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (76716126..76735770) | CF2R, HTR, PAR-1, PAR1, TR | 187930 |
ID: 5727 | patched 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95442980..95516971, complement) | BCNS, BCNS1, NBCCS, PTC, PTC1, PTCH | 601309 |
ID: 2623 | GATA binding protein 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (48786590..48794311) | CNSHA9, ERYF1, GATA-1, GF-1, GF1, HAEADA, NF-E1, NFE1, XLANP, XLTDA, XLTT | 305371 |
ID: 633 | biglycan [Homo sapiens (human)] | Chromosome X, NC_000023.11 (153494980..153509546) | DSPG1, MRLS, PG-S1, PGI, SEMDX, SLRR1A | 301870 |
ID: 10253 | sprouty RTK signaling antagonist 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (80335976..80341126, complement) | IGAN3, hSPRY2 | 602466 |
ID: 8013 | nuclear receptor subfamily 4 group A member 3 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (99821885..99866891) | CHN, CSMF, MINOR, NOR1 | 600542 |
ID: 3816 | kallikrein 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (50819146..50823787, complement) | KLKR, Klk6, hK1 | 147910 |
ID: 8087 | FMR1 autosomal homolog 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (180912670..180982753) | CMYO9A, CMYO9B, CMYP9A, CMYP9BP, MYOPMIL, MYORIBF, FXR1 | 600819 |
ID: 8431 | nuclear receptor subfamily 0 group B member 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (26911489..26913975, complement) | SHP, SHP1 | 604630 |
ID: 649 | bone morphogenetic protein 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22165372..22212326) | OI13, PCOLC, PCP, PCP2, TLD | 112264 |
ID: 5359 | phospholipid scramblase 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (146515180..146544607, complement) | MMTRA1B | 604170 |
ID: 3273 | histidine rich glycoprotein [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (186666014..186678234) | HPRGP, THPH11, HRG | 142640 |
ID: 3198 | homeobox A1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (27092993..27096000, complement) | BSAS, HOX1, HOX1F | 142955 |