Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 4137
  • Symbol: MAPT
  • Description: microtubule associated protein tau

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Disease_Term Source Rank Other Values
Supranuclear palsy, progressive atypical, 260540 (3) OMIM high
  • Genome region : 17q21.31
  • OMIM_ID : 157140 OMIM gene ID
  • OMIM_ID : 260540 OMIM phenotype ID
Pick disease, 172700 (3) OMIM high
  • Genome region : 14q24.2
  • Genome region : 17q21.31
  • OMIM_ID : 104311 OMIM gene ID
  • OMIM_ID : 157140 OMIM gene ID
  • OMIM_ID : 172700 OMIM phenotype ID
Supranuclear palsy, progressive, 601104 (3) OMIM high
  • Genome region : 17q21.31
  • OMIM_ID : 157140 OMIM gene ID
  • OMIM_ID : 601104 OMIM phenotype ID
{Parkinson disease, susceptibility to}, 168600 (3) OMIM high
  • Genome region : 17q21.31
  • Genome region : 4q23
  • Genome region : 6q27
  • OMIM_ID : 103730 OMIM gene ID
  • OMIM_ID : 157140 OMIM gene ID
  • OMIM_ID : 168600 OMIM phenotype ID
  • OMIM_ID : 600075 OMIM gene ID
Dementia, frontotemporal, with or without parkinsonism, 600274 (3) OMIM high
  • Genome region : 17q21.31
  • OMIM_ID : 157140 OMIM gene ID
  • OMIM_ID : 600274 OMIM phenotype ID
Parkinson's disease GWAS high
Bone mineral density GWAS high
Idiopathic pulmonary fibrosis GWAS high
Corticobasal degeneration GWAS high
Interstitial lung disease GWAS high
Progressive supranuclear palsy GWAS high
Intracranial volume GWAS high
Alzheimer's disease in APOE e4- carriers GWAS high
Subcortical brain region volumes GWAS high
Head circumference (infant) GWAS high