| ID: 1311 | cartilage oligomeric matrix protein [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (18782773..18791305, complement) | CTS2, EDM1, EPD1, MED, PSACH, THBS5, TSP-5, TSP5 | 600310 |
| ID: 10913 | ectodysplasin A receptor [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (108894471..108989220, complement) | DL, ECTD10A, ECTD10B, ED1R, ED3, ED5, EDA-A1R, EDA1R, EDA3, HRM1 | 604095 |
| ID: 4000 | lamin A/C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156082573..156140081) | CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL, FPLD, FPLD2, HGPS, IDC, LDP1, LFP, LGMD1B, LMN1, LMNC, LMNL1, MADA, PRO1 | 150330 |
| ID: 1836 | solute carrier family 26 member 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (149960758..149987400) | D5S1708, DTD, DTDST, EDM4, MST153, MSTP157 | 606718 |
| ID: 1896 | ectodysplasin A [Homo sapiens (human)] | Chromosome X, NC_000023.11 (69616113..70039472) | ECTD1, ED1, ED1-A1, ED1-A2-A1, EDA-A2, EDA1, EDA2, HED, HED1, ODT1, STHAGX1, TNLG7C, XHED, XLHED, EDA | 300451 |
| ID: 10804 | gap junction protein beta 6 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20221962..20232319, complement) | CX30, DFNA3, DFNA3B, DFNB1B, ECTD2, ED2, EDH, HED, HED2 | 604418 |
| ID: 203859 | anoctamin 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22192473..22283357) | GDD1, LGMD2L, LGMDR12, TMEM16E | 608662 |
| ID: 5818 | nectin cell adhesion molecule 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (119638098..119729200, complement) | CD111, CLPED1, ED4, HIgR, HV1S, HVEC, OFC7, PRR, PRR1, PVRL1, PVRR, PVRR1, SK-12, nectin-1 | 600644 |
| ID: 2697 | gap junction protein alpha 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (121435646..121449727) | AVSD3, CMDR, CX43, EKVP, EKVP3, GJAL, HLHS1, HSS, ODDD, PPKCA | 121014 |
| ID: 2316 | filamin A [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154348531..154374634, complement) | ABP-280, ABPX, CSBS, CVD1, FGS2, FLN, FLN-A, FLN1, FMD, MNS, NHBP, OPD, OPD1, OPD2, XLVD, XMVD | 300017 |
| ID: 497652 | adrenocortical dysplasia [Mus musculus (house mouse)] | Chromosome 8, NC_000074.7 (106424789..106427748, complement) | | |
| ID: 1280 | collagen type II alpha 1 chain [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (47972967..48006212, complement) | ANFH, AOM, COL11A3, SEDC, STL1 | 120140 |
| ID: 59341 | transient receptor potential cation channel subfamily V member 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109783087..109833398, complement) | BCYM3, CMT2C, HMSN2C, OTRPC4, SMAL, SPSMA, SSQTL1, TRP12, VRL2, VROAC | 605427 |
| ID: 2778 | GNAS complex locus [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (58839748..58911192) | AHO, C20orf451, GPSA, GSA, GSP, NESP, PITA3, POH, SCG6, SgVI, GNAS | 139320 |
| ID: 19206 | patched 1 [Mus musculus (house mouse)] | Chromosome 13, NC_000079.7 (63656142..63721274, complement) | A230106A15Rik, Ptc, Ptc1, Ptch, mes, wig | |
| ID: 2245 | FYVE, RhoGEF and PH domain containing 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (54445454..54496234, complement) | AAS, FGDY, MRXS16, ZFYVE3 | 300546 |
| ID: 4148 | matrilin 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (19992052..20012668, complement) | DIPOA, EDM5, HOA, OADIP, OS2, SEMDBCD | 602109 |
| ID: 65057 | ACD shelterin complex subunit and telomerase recruitment factor [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (67657512..67660260, complement) | PIP1, PTOP, TINT1, TPP1 | 609377 |
| ID: 128178 | EDAR associated via death domain [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (236348259..236484930) | CR, ECTD11A, ECTD11B, ED3, EDA3 | 606603 |
| ID: 109920 | cleidocranial dysplasia [Mus musculus (house mouse)] | | | |