Gene Expression: FOXP2

Gene Data

  • Gene Symbol: FOXP2
  • Gene ID: 93986
  • Synonyms: CAGH44, SPCH1, TNRC10
  • Description: forkhead box P2
  • Database Refs: HGNC:13875, MIM:605317, Ensembl:ENSG00000128573, HPRD:05611, Vega:OTTHUMG00000023131
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 31 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 59 diseases, scroll to view all:
  1. Alveolar rhabdomyosarcoma
  2. Autism
  3. Autism spectrum disease
  4. Axenfeld-Rieger syndrome
  5. Bamforth-Lazarus syndrome
  6. Blepharophimosis
  7. blepharophimosis, ptosis, and epicanthus
  8. Cancer
  9. Carbohydrate metabolism disease
  10. Cardiovascular system disease
  11. Central nervous system disease
  12. Corpus luteum cyst
  13. Developmental disease of mental health
  14. Diabetes mellitus
  15. Disease
  16. Disease of anatomical entity
  17. Disease of cellular proliferation
  18. Disease of mental health
  19. Disease of metabolism
  20. Dyslexia
  21. Endocrine pancreas disease
  22. Endocrine system disease
  23. Eye and adnexa disease
  24. Eye disease
  25. Eyelid disease
  26. Female reproductive system disease
  27. Gastrointestinal system disease
  28. Genetic disease
  29. Gilles de la Tourette syndrome
  30. Glaucoma
  31. Globe disease
  32. Glucose metabolism disease
  33. Juvenile glaucoma
  34. Learning disability
  35. Lymphatic system disease
  36. Lymphedema
  37. Monogenic disease
  38. Musculoskeletal system disease
  39. Nervous system disease
  40. Organ system cancer
  41. Ovarian cyst
  42. Ovarian disease
  43. Ovarian dysfunction
  44. Pancreas disease
  45. Pervasive developmental disease
  46. Premature ovarian failure
  47. Reading disease
  48. Reproductive system disease
  49. Retinal degeneration
  50. Retinal disease
  51. Rhabdomyosarcoma
  52. Rolandic epilepsy
  53. Sensory system disease
  54. Skeletal muscle cancer
  55. Skin and subcutaneous tissue disease
  56. Soft tissue disease
  57. Specific developmental disease
  58. Tic disease
  59. Tissue disease

Stage Associations

This gene is associated with the following stages: