TTN wt Allele

Human TTN wild-type allele is located in the vicinity of 2q31 and is approximately 305 kb in length. This allele, which encodes titin protein, is involved in both muscle filament structure and protein phosphorylation. Mutation of the gene is associated with hereditary myopathy with early respiratory failure, familial hypertrophic cardiomyopathy type 9, cardiomyopathy dilated type 1G, tardive tibial muscular dystrophy, limb-girdle muscular dystrophy type 2J and early-onset myopathy with fatal cardiomyopathy. (NCI Thesaurus)

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TTN Gene

This gene plays a role in sarcomere structure.

TTMB

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TTL wt Allele

Human TTL wild-type allele is located in the vicinity of 2q13 and is approximately 50 kb in length. This allele, which encodes…

TTL Gene

This gene is involved in tubulin modification.

TTK wt Allele

Human TTK wild-type allele is located within 6q13-q21 is approximately 38 kb in length. This allele, which encodes dual specificity protein kinase…

TTK Gene

This gene is involved in cell cycle checkpoint regulation.