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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