TTN Chromosome 2

Titin
7833 variants 7833 Health Risk

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What This Gene Does
This gene encodes a large abundant protein of striated muscle. The product of this gene is divided into two regions, a N-terminal I-band and a C-terminal A-band. The I-band, which is the elastic part of the molecule, contains two regions of tandem immunoglobulin domains on either side of a PEVK region that is rich in proline, glutamate, valine and lysine. The A-band, which is thought to act as a protein-ruler, contains a mixture of immunoglobulin and fibronectin repeats, and possesses kinase activity. An N-terminal Z-disc region and a C-terminal M-line region bind to the Z-line and M-line of the sarcomere, respectively, so that a single titin molecule spans half the length of a sarcomere. Titin also contains binding sites for muscle associated proteins so it serves as an adhesion template for the assembly of contractile machinery in muscle cells. It has also been identified as a structural protein for chromosomes. Alternative splicing of this gene results in multiple transcript variants. Considerable variability exists in the I-band, the M-line and the Z-disc regions of titin. Variability in the I-band region contributes to the differences in elasticity of different titin isoforms and, therefore, to the differences in elasticity of different muscle types. Mutations in this gene are associated with familial hypertrophic cardiomyopathy 9, and autoantibodies to titin are produced in patients with the autoimmune disease scleroderma. [provided by RefSeq, Feb 2012]
Gene Info
Gene Group
"Fibronectin type III domain containing|I-set domain containing|Myosin light chain kinase family"
Locus Type
gene with protein product
Location
2q31.2
Ensembl
ENSG00000155657
Associated Conditions (130)
Dilated cardiomyopathy 1G
Autosomal recessive limb-girdle muscular dystrophy type 2J
Cardiovascular phenotype
Hypertrophic cardiomyopathy 9
Myopathy
myofibrillar
9
with early respiratory failure
Tibial muscular dystrophy
Early-onset myopathy with fatal cardiomyopathy
Cardiomyopathy
TTN-related disorder
6 conditions
Primary dilated cardiomyopathy
Hypertrophic cardiomyopathy
Long QT syndrome
Areflexia of lower limbs
Spinal rigidity
Thoracic kyphoscoliosis
Bilateral talipes equinovarus
+110 more conditions
Key Variants
RS1004455055
Conflicting classifications of pathogenicity
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Cardiovascular phenotype
Health Risk
RS1005082526
Conflicting classifications of pathogenicity
Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J
Health Risk
RS1006806821
Conflicting classifications of pathogenicity
Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Myopathy
Health Risk
RS1007434751
Conflicting classifications of pathogenicity
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G
Health Risk
RS1010541689
Conflicting classifications of pathogenicity
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G
Health Risk
RS1012929202
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G
Health Risk
RS1015506783
Conflicting classifications of pathogenicity
Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Cardiovascular phenotype
Health Risk
RS1016165797
Conflicting classifications of pathogenicity
Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Cardiomyopathy
Health Risk
RS10200398
Conflicting classifications of pathogenicity
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy
Health Risk
RS1020838415
Conflicting classifications of pathogenicity
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G
Health Risk
RS1021499065
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS1023726354
Conflicting classifications of pathogenicity
Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J
Health Risk
All Variants (7833)
RSID Category Clinical Significance Conditions
RS763029699 Health Risk Conflicting classifications of pathogenicity
RS763065439 Health Risk Conflicting classifications of pathogenicity See cases, See cases
RS763098227 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Cardiomyopathy
RS763205133 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Early-onset myopathy with fatal cardiomyopathy
RS763212024 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS763242057 Health Risk Conflicting classifications of pathogenicity
RS763270971 Health Risk Conflicting classifications of pathogenicity Early-onset myopathy with fatal cardiomyopathy, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G
RS763279178 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiomyopathy
RS763336230 Health Risk Conflicting classifications of pathogenicity Early-onset myopathy with fatal cardiomyopathy, Myopathy, myofibrillar
RS763361422 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J
RS763404256 Health Risk Conflicting classifications of pathogenicity Primary dilated cardiomyopathy, Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J
RS763629416 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G
RS763668057 Health Risk Conflicting classifications of pathogenicity Tibial muscular dystrophy, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G
RS763682832 Health Risk Conflicting classifications of pathogenicity Myopathy, myofibrillar, 9
RS763685410 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, TTN-related disorder
RS763711863 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1G, Myopathy, myofibrillar
RS763722868 Health Risk Conflicting classifications of pathogenicity
RS763729258 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS763733251 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J
RS763742779 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Cardiomyopathy
RS763833161 Health Risk Conflicting classifications of pathogenicity
RS763845436 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Arrhythmogenic right ventricular cardiomyopathy
RS763871350 Health Risk Conflicting classifications of pathogenicity
RS764035021 Health Risk Conflicting classifications of pathogenicity
RS764059405 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Tibial muscular dystrophy
RS764179161 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, TTN-related disorder
RS764189986 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1G, Myopathy, myofibrillar
RS764231632 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Cardiovascular phenotype
RS764245090 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Cardiomyopathy
RS764248656 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Early-onset myopathy with fatal cardiomyopathy
RS764250397 Health Risk Conflicting classifications of pathogenicity
RS764254441 Health Risk Conflicting classifications of pathogenicity
RS764263517 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Myopathy, myofibrillar
RS764333790 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy, Tibial muscular dystrophy
RS764363274 Health Risk Conflicting classifications of pathogenicity Tibial muscular dystrophy, Myopathy, myofibrillar
RS764388462 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Cardiovascular phenotype
RS764394936 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G
RS764437671 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Cardiovascular phenotype
RS764487443 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G
RS764521300 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiomyopathy
RS764544769 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Tibial muscular dystrophy, Myopathy
RS764561909 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, 6 conditions
RS764568599 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Cardiovascular phenotype
RS764670848 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy
RS764687326 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, 6 conditions
RS764777213 Health Risk Conflicting classifications of pathogenicity Myopathy, myofibrillar, 9
RS764819788 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Cardiovascular phenotype
RS764832849 Health Risk Conflicting classifications of pathogenicity
RS764873258 Health Risk Conflicting classifications of pathogenicity Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Cardiovascular phenotype
RS764882950 Health Risk Conflicting classifications of pathogenicity Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Cardiomyopathy
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