| P594 | Ensembl gene ID | ENSG00000181027 |
| P704 | Ensembl transcript ID | ENST00000318584 |
| ENST00000391909 | ||
| ENST00000593800 | ||
| ENST00000593875 | ||
| ENST00000593877 | ||
| ENST00000593902 | ||
| ENST00000593995 | ||
| ENST00000594467 | ||
| ENST00000595570 | ||
| ENST00000595868 | ||
| ENST00000596460 | ||
| ENST00000596974 | ||
| ENST00000597313 | ||
| ENST00000597339 | ||
| ENST00000597403 | ||
| ENST00000598271 | ||
| ENST00000600005 | ||
| ENST00000600227 | ||
| ENST00000600629 | ||
| ENST00000600646 | ||
| ENST00000600681 | ||
| ENST00000600834 | ||
| ENST00000600872 | ||
| ENST00000600977 | ||
| ENST00000601299 | ||
| ENST00000602181 | ||
| ENST00000602250 | ||
| P351 | Entrez Gene ID | 79147 |
| P2888 | exact match | http://identifiers.org/ncbigene/79147 |
| P353 | HGNC gene symbol | FKRP |
| P354 | HGNC ID | 17997 |
| P593 | HomoloGene ID | 11513 |
| P492 | OMIM ID | 606596 |
| 606596 | ||
| P639 | RefSeq RNA ID | NM_001039885 |
| NM_024301 | ||
| XM_005259247 | ||
| XM_005259248 | ||
| XM_005259249 | ||
| XM_011527306 | ||
| XM_011527307 | ||
| XM_017027297 | ||
| XM_024451707 | ||
| P2892 | UMLS CUI | C1425226 |
| P1057 | chromosome | human chromosome 19 | Q510786 |
| P4196 | cytogenetic location | 19q13.32 | |
| P688 | encodes | Fukutin-related protein | Q21117917 |
| Fukutin related protein | Q22683586 | ||
| P5572 | expressed in | anterior pituitary | Q356002 |
| right coronary artery | Q429285 | ||
| gastrocnemius muscle | Q943203 | ||
| sural nerve | Q6135922 | ||
| apex of heart | Q66502809 | ||
| cardiac muscle tissue of right atrium | Q66502871 | ||
| myocardium of left ventricle | Q66504996 | ||
| left uterine tube | Q66509809 | ||
| muscle of thigh | Q66514508 | ||
| stromal cell of endometrium | Q66592424 | ||
| P703 | found in taxon | Homo sapiens | Q15978631 |
| P2293 | genetic association | autosomal recessive limb-girdle muscular dystrophy type 2I | Q22965446 |
| congenital muscular dystrophy with cerebellar involvement | Q56014127 | ||
| congenital muscular dystrophy with intellectual disability | Q56014128 | ||
| congenital muscular dystrophy without intellectual disability | Q56014129 | ||
| P645 | genomic end | 46776988 | |
| 47280245 | |||
| P644 | genomic start | 46746046 | |
| 47249303 | |||
| P684 | ortholog | Fkrp | Q18299181 |
| Fkrp | Q24412974 | ||
| CG15651 | Q29732871 | ||
| fkrp | Q29777063 | ||
| P2548 | strand orientation | forward strand | Q22809680 |