| ID: 150084 | immunoglobulin superfamily member 5 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39711771..39802081) | GSF5, JAM4 | 610638 |
| ID: 4851 | notch receptor 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136494433..136546048, complement) | AOS5, AOVD1, TAN1, hN1 | 190198 |
| ID: 2908 | nuclear receptor subfamily 3 group C member 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (143277931..143435512, complement) | GCCR, GCR, GCRST, GR, GRL | 138040 |
| ID: 3949 | low density lipoprotein receptor [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (11089463..11133820) | FH, FHC, FHCL1, LDLCQ2 | 606945 |
| ID: 4854 | notch receptor 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (15159038..15200995, complement) | CADASIL, CADASIL1, CASIL, IMF2, LMNS | 600276 |
| ID: 4853 | notch receptor 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (119911553..120069662, complement) | AGS2, HJCYS, hN2 | 600275 |
| ID: 9223 | membrane associated guanylate kinase, WW and PDZ domain containing 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (65353526..66038918, complement) | AIP-3, AIP3, BAIAP1, BAP-1, BAP1, MAGI-1, MAGI-1b, Magi1d, TNRC19, WWP3 | 602625 |
| ID: 4038 | LDL receptor related protein 4 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (46856717..46918550, complement) | CLSS, CMS17, LRP-4, LRP10, MEGF7, SOST2 | 604270 |
| ID: 84708 | ligand of numb-protein X 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (53459301..53652477, complement) | LNX, MPDZ, PDZRN2 | 609732 |
| ID: 23178 | PAS domain containing serine/threonine kinase [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241106099..241150347, complement) | PASKIN, STK37 | 607505 |
| ID: 222484 | ligand of numb-protein X 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27545913..27621107, complement) | PDZRN1 | 609733 |
| ID: 79174 | cysteine rich with EGF like domains 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (49918634..49927537) | | 607171 |
| ID: 10443 | NEDD4 binding protein 2 like 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (32432485..32538868, complement) | 92M18.3, CG005, CG016, PFAAP5 | 615788 |