History:GENE:HLTF    GENE:RUNX1    

Gene Expression: MAPT

Gene Data

  • Gene Symbol: MAPT
  • Gene ID: 4137
  • Synonyms: DDPAC, FTDP-17, MAPTL, MSTD, MTBT1, MTBT2, PPND, TAU
  • Description: microtubule-associated protein tau
  • Database Refs: HGNC:6893, MIM:157140, Ensembl:ENSG00000186868, HPRD:01142, Vega:OTTHUMG00000168833
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 1 out of 30 exons in this gene. (More about DEXSeq here)

Cluster Associations

This gene is associated with the following clusters:

Disease Associations

This gene is associated with the following diseases. Clicking on the disease will take you to the disease association entry for that disease.

This gene is associated with 73 diseases, scroll to view all:
  1. Agnosia
  2. Alzheimer's disease
  3. Amyotrophic lateral sclerosis
  4. Anterior horn cell disease
  5. Aphasia
  6. Apraxia
  7. Basal ganglia disease
  8. Brain disease
  9. Cancer
  10. Cardiovascular system disease
  11. Central nervous system disease
  12. Central nervous system hereditary degene
  13. Cerebral arterial disease
  14. Cerebral degeneration
  15. Cerebrovascular accident
  16. Cerebrovascular disease
  17. Chromosomal disease
  18. Cognitive disease
  19. Communication disease
  20. Dementia
  21. Developmental disease of mental health
  22. Disease
  23. Disease of anatomical entity
  24. Disease of cellular proliferation
  25. Disease of mental health
  26. Down syndrome
  27. Frontotemporal dementia
  28. Heart disease
  29. Ideomotor apraxia
  30. Intellectual disability
  31. Intracranial arterial disease
  32. Intracranial arteriosclerosis
  33. Ischemia
  34. Kluver-Bucy syndrome
  35. Language disease
  36. Leukodystrophy
  37. Lewy body dementia
  38. Lissencephaly
  39. Malignant glioma
  40. Motor neuron disease
  41. Movement disease
  42. Multiple system atrophy
  43. Muscle tissue disease
  44. Muscular disease
  45. Musculoskeletal system disease
  46. Mutism
  47. Myopathy
  48. Myotonic disease
  49. Myotonic dystrophy
  50. Neoplasm of autonomic nervous system
  51. Nervous system cancer
  52. Nervous system disease
  53. Neuroblastoma
  54. Neurodegenerative disease
  55. Neuromuscular disease
  56. Neuropathy
  57. Normal pressure hydrocephalus
  58. Organ system cancer
  59. Parkinson's disease
  60. Peripheral nervous system neoplasm
  61. Pick's disease
  62. Postencephalitic Parkinson disease
  63. Prion disease
  64. Progressive supranuclear palsy
  65. Prosopagnosia
  66. Psychomotor disease
  67. Secondary Parkinson disease
  68. Specific developmental disease
  69. Speech disease
  70. Tauopathy
  71. Toxic encephalopathy
  72. Vascular dementia
  73. Vascular disease

Stage Associations

This gene is associated with the following stages: