| ID: 8742 | TNF superfamily member 12 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7549058..7557881) | APO3L, DR3LG, TNLG4A, TWEAK | 602695 |
| ID: 407977 | TNFSF12-TNFSF13 readthrough [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7549058..7561601) | TWE-PRIL | |
| ID: 23125 | calmodulin binding transcription activator 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (4967997..4987675, complement) | | 611508 |
| ID: 657 | bone morphogenetic protein receptor type 1A [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86755763..86932844) | 10q23del, ACVRLK3, ALK-3, ALK3, BMPR-1A, CD292, SKR5 | 601299 |
| ID: 23555 | tetraspanin 15 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (69451465..69549508) | 2700063A19Rik, NET-7, NET7, TM4SF15 | 613140 |
| ID: 169436 | serine/threonine kinase like domain containing 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133376366..133406096) | C9orf96, SgK071, Sk521 | 618530 |
| ID: 55638 | syntabulin [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (109573978..109691600, complement) | GOLSYN, OCSYN, SNPHL | 611568 |
| ID: 92912 | ubiquitin conjugating enzyme E2 Q2 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (75843447..75901078) | | 612501 |
| ID: 54662 | TBC1 domain family member 13 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128787253..128810430) | | 616218 |
| ID: 64423 | inverted formin 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (104689618..104722535) | C14orf151, C14orf173, CMTDIE, FSGS5, pp9484 | 610982 |
| ID: 7466 | wolframin ER transmembrane glycoprotein [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (6269850..6303265) | CTRCT41, WFRS, WFS, WFSL | 606201 |
| ID: 7168 | tropomyosin 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (63042747..63071915) | C15orf13, CMD1Y, CMH3, HEL-S-265, HTM-alpha, LVNC9, TMSA | 191010 |