| OBSCN | 
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| | Available structures | 
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 | PDB | Ortholog search: PDBe RCSB | 
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 | | List of PDB id codes | 
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 | 1V1C, 2CR6, 2DKU, 2DM7, 2E7B, 2EDF, 2EDH, 2EDL, 2EDQ, 2EDR, 2EDT, 2EDW, 2ENY, 2EO1, 2GQH, 2YZ8, 4C4K, 2MWC, 4RSV, 2N56 | 
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| Identifiers | 
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| Aliases | OBSCN, ARHGEF30, UNC89, obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF | 
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| External IDs | OMIM: 608616; MGI: 2681862; HomoloGene: 70869; GeneCards: OBSCN; OMA:OBSCN - orthologs | 
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|  | 
| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 11 (mouse) | 
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 |  |  | Band | 11|11 B1.3 | Start | 58,885,082 bp | 
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 | End | 59,029,996 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | muscle of thigh
 apex of heart
 gastrocnemius muscle
 Skeletal muscle tissue of rectus abdominis
 right auricle of heart
 left ventricle
 body of tongue
 biceps brachii
 Skeletal muscle tissue of biceps brachii
 right hemisphere of cerebellum
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 | | Top expressed in |  | muscle of thigh
 myocardium of ventricle
 knee joint
 skeletal muscle tissue
 interventricular septum
 triceps brachii muscle
 quadriceps femoris muscle
 temporal muscle
 digastric muscle
 extraocular muscle
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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Obscurin is a protein that in humans is encoded by the OBSCN gene. Obscurin belongs to the family of giant sarcomeric signaling proteins that includes titin and nebulin. Obscurin is expressed in cardiac and skeletal muscle, and plays a role in the organization of myofibrils during sarcomere assembly. A mutation in the OBSCN gene has been associated with hypertrophic cardiomyopathy and altered obscurin protein properties have been associated with other muscle diseases.