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Gene Expression: FOXL2

Gene Data

  • Gene Symbol: FOXL2
  • Gene ID: 668
  • Synonyms: BPES, BPES1, PFRK, PINTO, POF3
  • Description: forkhead box L2
  • Database Refs: HGNC:1092, MIM:605597, Ensembl:ENSG00000183770, HPRD:05723, Vega:OTTHUMG00000159889
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 1 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 43 diseases, scroll to view all:
  1. Amblyopia
  2. Amenorrhea
  3. Blepharophimosis
  4. blepharophimosis, ptosis, and epicanthus
  5. Brachial plexus neuritis
  6. Congenital nervous system abnormality
  7. Corpus luteum cyst
  8. Developmental disease of mental health
  9. Disease
  10. Disease of anatomical entity
  11. Eyelid disease
  12. Female reproductive system disease
  13. Female reproductve organ cancer
  14. Genetic disease
  15. Genetic disorder
  16. Gonadal dysgenesis
  17. Gonadoblastoma
  18. Granulosa cell tumor
  19. Hypertropia
  20. Infertility
  21. Intellectual disability
  22. Juvenile type testicular granulosa cell
  23. Laryngostenosis
  24. Medical disorder
  25. Microcephaly
  26. Mobius syndrome
  27. Monogenic disease
  28. Musculoskeletal system disease
  29. Ovarian cancer
  30. Ovarian cyst
  31. Ovarian disease
  32. Ovarian dysfunction
  33. Physical disorder
  34. Premature ovarian failure
  35. Reproductive system disease
  36. Sex cord-gonadal stromal tumor
  37. Skin and subcutaneous tissue disease
  38. Soft tissue disease
  39. Specific developmental disease
  40. Steatitis
  41. Syndrome
  42. Testicular granulosa cell tumor
  43. Tissue disease

Stage Associations

This gene is associated with the following stages: