| ID: 8291 | dysferlin [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (71453154..71686763) | FER1L1, LGMD2B, LGMDR2, MMD1 | 603009 |
| ID: 2218 | fukutin [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (105558117..105655950) | CMD1X, FCMD, LGMD2M, LGMDR13, MDDGA4, MDDGB4, MDDGC4 | 607440 |
| ID: 4000 | lamin A/C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156082546..156140089) | CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL, FPLD, FPLD2, HGPS, IDC, LDP1, LFP, LGMD1B, LMN1, LMNC, LMNL1, MADA, PRO1 | 150330 |
| ID: 6443 | sarcoglycan beta [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (52020695..52038319, complement) | A3b, LGMD2E, LGMDR4, SGC | 600900 |
| ID: 3106 | major histocompatibility complex, class I, B [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31353866..31357245, complement) | AS, B-4901, HLAB | 142830 |
| ID: 1756 | dystrophin [Homo sapiens (human)] | Chromosome X, NC_000023.11 (31119219..33339609, complement) | BMD, CMD3B, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272, MRX85 | 300377 |
| ID: 23534 | transportin 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128954180..129055173, complement) | IPO12, LGMD1F, LGMDD2, MTR10A, TRN-SR, TRN-SR2, TRNSR | 610032 |
| ID: 8557 | titin-cap [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (39665346..39666554) | CMD1N, CMH25, LGMD2G, LGMDR7, T-cap, TELE, telethonin | 604488 |
| ID: 2483 | FSHD region gene 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (189940819..189963204) | FRG1A, FSG1 | 601278 |
| ID: 6442 | sarcoglycan alpha [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50165517..50175932) | 50DAG, ADL, DAG2, DMDA2, LGMD2D, LGMDR3, SCARMD1, adhalin | 600119 |
| ID: 79147 | fukutin related protein [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46746015..46758575) | LGMD2I, LGMDR9, MDC1C, MDDGA5, MDDGB5, MDDGC5 | 606596 |
| ID: 1605 | dystroglycan 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49468703..49535618) | 156DAG, A3a, AGRNR, DAG, LGMDR16, MDDGA9, MDDGC7, MDDGC9 | 128239 |
| ID: 3105 | major histocompatibility complex, class I, A [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (29942470..29945884) | HLAA | 142800 |
| ID: 10585 | protein O-mannosyltransferase 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (131502902..131523806) | LGMD2K, LGMDR11, MDDGA1, MDDGB1, MDDGC1, RT | 607423 |
| ID: 7157 | tumor protein p53 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7668402..7687550, complement) | BCC7, BMFS5, LFS1, P53, TRP53 | 191170 |
| ID: 5339 | plectin [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143915147..143976800, complement) | EBS1, EBSMD, EBSND, EBSO, EBSOG, EBSPA, HD1, LGMD2Q, LGMDR17, PCN1, PLEC1b, PLTN, PLEC | 601282 |
| ID: 7273 | titin [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (178525989..178807423, complement) | CMD1G, CMH9, CMPD4, EOMFC, HMERF, LGMD2J, LGMDR10, MYLK5, SALMY, TMD | 188840 |
| ID: 825 | calpain 3 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (42359500..42412317) | CANP3, CANPL3, LGMD2, LGMD2A, LGMDD4, LGMDR1, nCL-1, p94 | 114240 |
| ID: 9215 | LARGE xylosyl- and glucuronyltransferase 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (33162237..33922841, complement) | LARGE, MDC1D, MDDGA6, MDDGB6 | 603590 |
| ID: 2489 | facioscapulohumeral muscular dystrophy 1A [Homo sapiens (human)] | | FMD, FSHD, FSHD1A, FSHMD | 158900 |