Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:7273
  • Symbol:TTN
  • Description:titin

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Disease_Term Source Rank Other Values
Tibial muscular dystrophy, tardive, 600334 (3) OMIM high
  • Genome region :2q31.2
  • OMIM_ID :188840OMIM gene ID
  • OMIM_ID :600334OMIM phenotype ID
Cardiomyopathy, dilated, 1G, 604145 (3) OMIM high
  • Genome region :2q31.2
  • OMIM_ID :188840OMIM gene ID
  • OMIM_ID :604145OMIM phenotype ID
Myopathy, proximal, with early respiratory muscle involvement, 603689 (3) OMIM high
  • Genome region :2q31.2
  • OMIM_ID :188840OMIM gene ID
  • OMIM_ID :603689OMIM phenotype ID
Cardiomyopathy, familial hypertrophic, 9, 613765 (3) OMIM high
  • Genome region :2q31.2
  • OMIM_ID :188840OMIM gene ID
  • OMIM_ID :613765OMIM phenotype ID
Muscular dystrophy, limb-girdle, type 2J, 608807 (3) OMIM high
  • Genome region :2q31.2
  • OMIM_ID :188840OMIM gene ID
  • OMIM_ID :608807OMIM phenotype ID
Myopathy, early-onset, with fatal cardiomyopathy, 611705 (3) OMIM high
  • Genome region :2q31.2
  • OMIM_ID :188840OMIM gene ID
  • OMIM_ID :611705OMIM phenotype ID
QT interval GWAS high
Rapid functional decline in sporadic amyotrophic lateral sclerosis GWAS high
Breast size GWAS high