| ID: 340267 | collagen type XXVIII alpha 1 chain [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (7338194..7543870, complement) | COL28 | 609996 |
| ID: 2660 | myostatin [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (190055700..190062729, complement) | GDF8, MSLHP | 601788 |
| ID: 340359 | kelch like family member 38 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123644442..123653801, complement) | C8ORFK36 | |
| ID: 286006 | leucine rich single-pass membrane protein 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (112480304..112491062) | C7orf53 | |
| ID: 844 | calsequestrin 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160190575..160201886) | CASQ, CSQ1, PDIB1, VMCQA | 114250 |
| ID: 270 | adenosine monophosphate deaminase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (114673098..114695546, complement) | MAD, MADA, MMDD | 102770 |
| ID: 115701 | alpha kinase 2 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (58481247..58629091, complement) | HAK | 619965 |
| ID: 4703 | nebulin [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (151485339..151734476, complement) | AMC6177D, NEM2, NEB | 161650 |
| ID: 84319 | cms1 ribosomal small subunit homolog [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (99817862..100181732) | C3orf26 | |
| ID: 253017 | trans-2,3-enoyl-CoA reductase like [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (64276298..64409460, complement) | CPVT3, GPSN2L, SRD5A2L2, TERL | 617242 |
| ID: 6588 | sarcolipin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107707378..107712056, complement) | | 602203 |
| ID: 5236 | phosphoglucomutase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (63593411..63660245) | CDG1T, GSD14 | 171900 |
| ID: 285525 | Yip1 domain family member 7 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (44622088..44662199, complement) | FinGER9, YIPFalpha1b, Yip1b | 619754 |
| ID: 5224 | phosphoglycerate mutase 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (44062727..44065567, complement) | GSD10, PGAM-M, PGAMM | 612931 |
| ID: 84700 | myosin XVIIIB [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (25742188..26063847) | KFS4 | 607295 |