OBSCN Chromosome 1

Obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF
90 variants 90 Health Risk

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What This Gene Does
The obscurin gene spans more than 150 kb, contains over 80 exons and encodes a protein of approximately 720 kDa. The encoded protein contains 68 Ig domains, 2 fibronectin domains, 1 calcium/calmodulin-binding domain, 1 RhoGEF domain with an associated PH domain, and 2 serine-threonine kinase domains. This protein belongs to the family of giant sacromeric signaling proteins that includes titin and nebulin, and may have a role in the organization of myofibrils during assembly and may mediate interactions between the sarcoplasmic reticulum and myofibrils. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Fibronectin type III domain containing|I-set domain containing|Dbl family Rho GEFs|Myosin light chain kinase family"
Locus Type
gene with protein product
Location
1q42.13
Ensembl
ENSG00000154358
Associated Conditions (8)
OBSCN-related disorder
Rhabdomyolysis
susceptibility to
1
Inborn genetic diseases
Short stature
Hearing loss
autosomal recessive 120
Key Variants
All Variants (90)
RSID Category Clinical Significance Conditions
RS113760892 Health Risk Conflicting classifications of pathogenicity OBSCN-related disorder, OBSCN-related disorder
RS1284658608 Health Risk Conflicting classifications of pathogenicity —
RS139306713 Health Risk Conflicting classifications of pathogenicity —
RS1433965473 Health Risk Conflicting classifications of pathogenicity —
RS185531813 Health Risk Conflicting classifications of pathogenicity —
RS191837710 Health Risk Conflicting classifications of pathogenicity OBSCN-related disorder, OBSCN-related disorder
RS193302438 Health Risk Conflicting classifications of pathogenicity Rhabdomyolysis, susceptibility to, 1
RS199704824 Health Risk Conflicting classifications of pathogenicity —
RS199979779 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS199985706 Health Risk Conflicting classifications of pathogenicity —
RS200058427 Health Risk Conflicting classifications of pathogenicity —
RS200870329 Health Risk Conflicting classifications of pathogenicity —
RS201097669 Health Risk Conflicting classifications of pathogenicity —
RS201224400 Health Risk Conflicting classifications of pathogenicity —
RS201231167 Health Risk Conflicting classifications of pathogenicity —
RS201366506 Health Risk Conflicting classifications of pathogenicity —
RS202143056 Health Risk Conflicting classifications of pathogenicity —
RS367752269 Health Risk Conflicting classifications of pathogenicity —
RS368175234 Health Risk Conflicting classifications of pathogenicity —
RS374013818 Health Risk Conflicting classifications of pathogenicity —
RS375459972 Health Risk Conflicting classifications of pathogenicity —
RS375723852 Health Risk Conflicting classifications of pathogenicity —
RS376500523 Health Risk Conflicting classifications of pathogenicity —
RS536227878 Health Risk Conflicting classifications of pathogenicity Rhabdomyolysis, susceptibility to, 1
RS545019561 Health Risk Conflicting classifications of pathogenicity Rhabdomyolysis, susceptibility to, 1
RS547447722 Health Risk Conflicting classifications of pathogenicity —
RS548710709 Health Risk Conflicting classifications of pathogenicity —
RS55939441 Health Risk Conflicting classifications of pathogenicity OBSCN-related disorder, OBSCN-related disorder
RS562324692 Health Risk Conflicting classifications of pathogenicity —
RS563377499 Health Risk Conflicting classifications of pathogenicity —
RS569260441 Health Risk Conflicting classifications of pathogenicity —
RS71180793 Health Risk Conflicting classifications of pathogenicity OBSCN-related disorder, OBSCN-related disorder
RS749702058 Health Risk Conflicting classifications of pathogenicity —
RS750723281 Health Risk Conflicting classifications of pathogenicity —
RS753928558 Health Risk Conflicting classifications of pathogenicity —
RS755253225 Health Risk Conflicting classifications of pathogenicity —
RS758211855 Health Risk Conflicting classifications of pathogenicity —
RS759680619 Health Risk Conflicting classifications of pathogenicity —
RS759751670 Health Risk Conflicting classifications of pathogenicity —
RS761994990 Health Risk Conflicting classifications of pathogenicity OBSCN-related disorder, OBSCN-related disorder
RS764679750 Health Risk Conflicting classifications of pathogenicity —
RS769496430 Health Risk Conflicting classifications of pathogenicity —
RS770355592 Health Risk Conflicting classifications of pathogenicity —
RS771719843 Health Risk Conflicting classifications of pathogenicity —
RS772551661 Health Risk Conflicting classifications of pathogenicity —
RS773797780 Health Risk Conflicting classifications of pathogenicity —
RS779774732 Health Risk Conflicting classifications of pathogenicity —
RS780502525 Health Risk Conflicting classifications of pathogenicity —
RS947434915 Health Risk Conflicting classifications of pathogenicity —
RS1005463281 Health Risk Likely pathogenic —
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