History:GENE:HSPA4    

Gene Expression: FGFR2

Gene Data

  • Gene Symbol: FGFR2
  • Gene ID: 2263
  • Synonyms: BBDS, BEK, BFR-1, CD332, CEK3, CFD1, ECT1, JWS, K-SAM, KGFR, TK14, TK25
  • Description: fibroblast growth factor receptor 2
  • Database Refs: HGNC:3689, MIM:176943, Ensembl:ENSG00000066468, HPRD:01492, Vega:OTTHUMG00000019175
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 3 out of 29 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 70 diseases, scroll to view all:
  1. Acanthosis nigricans
  2. Achondroplasia
  3. Acrocephalosyndactylia
  4. Adenocarcinoma
  5. Ankylosis
  6. Antley-Bixler syndrome
  7. Beare-Stevenson cutis gyrata syndrome
  8. Bone development disease
  9. Bone disease
  10. Breast cancer
  11. Cancer
  12. Carcinoma
  13. Cell type cancer
  14. Cerebral degeneration
  15. Cervical keratinizing squamous cell carc
  16. Choanal atresia
  17. Cholesteatoma
  18. Cleft palate
  19. Craniosynostosis
  20. Crouzon syndrome
  21. Dermatitis
  22. Disease
  23. Disease of anatomical entity
  24. Disease of cellular proliferation
  25. Dysostosis
  26. Endometrial cancer
  27. Endometrial carcinoma
  28. estrogen-receptor positive breast cancer
  29. Exophthalmos
  30. Eye and adnexa disease
  31. Eye disease
  32. Female reproductve organ cancer
  33. Gastrointestinal system cancer
  34. Genetic disease
  35. Genitourinary cancer
  36. Globe disease
  37. Hydrocephalus
  38. Hypertropia
  39. Hypochondroplasia
  40. Hypospadias
  41. Integumentary system disease
  42. Intestinal atresia
  43. Intracranial hypertension
  44. Kallmann syndrome
  45. Keratosis
  46. LADD syndrome
  47. Male reproductive organ cancer
  48. Medical disorder
  49. Monogenic disease
  50. Musculoskeletal system disease
  51. Nervous system disease
  52. Organ system cancer
  53. Orofacial cleft
  54. Osteochondrodysplasia
  55. Pfeiffer syndrome
  56. Physical disorder
  57. Prostate cancer
  58. Radioulnar synostosis
  59. Renal agenesis
  60. Reproductive organ cancer
  61. Saethre-Chotzen syndrome
  62. Sensory system disease
  63. Skin disease
  64. Squamous cell carcinoma
  65. Syndactyly
  66. Synostosis
  67. Thanatophoric dysplasia
  68. Thoracic cancer
  69. Uterine cancer
  70. Uterine neoplasm

Stage Associations

This gene is associated with the following stages: