Obscurin

OBSCN
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesOBSCN, ARHGEF30, UNC89, obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF
External IDsOMIM: 608616; MGI: 2681862; HomoloGene: 70869; GeneCards: OBSCN; OMA:OBSCN - orthologs
Orthologs
SpeciesHumanMouse
Entrez

84033

380698

Ensembl

ENSG00000154358

ENSMUSG00000061462

UniProt

Q5VST9

A2AAJ9

RefSeq (mRNA)

NM_001098623
NM_001271223
NM_052843
NM_001386125

NM_001171512
NM_199152

RefSeq (protein)

NP_001092093
NP_001258152
NP_443075

NP_001164983
NP_954603

Location (UCSC)Chr 1: 228.21 – 228.38 MbChr 11: 58.89 – 59.03 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

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.