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
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
Supranuclear palsy, progressive atypical, 260540 (3) OMIM high
  • Genome region : 17q21.31
  • OMIM_ID : 157140 OMIM gene ID
  • OMIM_ID : 260540 OMIM phenotype ID
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
Parkinson's disease GWAS high
Bone mineral density GWAS high
Idiopathic pulmonary fibrosis GWAS high