Gene Expression: FGFR3

Gene Data

  • Gene Symbol: FGFR3
  • Gene ID: 2261
  • Synonyms: ACH, CD333, CEK2, HSFGFR3EX, JTK4
  • Description: fibroblast growth factor receptor 3
  • Database Refs: HGNC:3690, MIM:134934, Ensembl:ENSG00000068078, HPRD:00624, Vega:OTTHUMG00000121148
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 2 out of 22 exons in this gene. (More about DEXSeq here)

Cluster Associations

This gene is associated with the following clusters: No Clusters were found

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 68 diseases, scroll to view all:
  1. Acanthosis nigricans
  2. Achondroplasia
  3. Acrocephalosyndactylia
  4. B-cell lymphocytic neoplasm
  5. Beare-Stevenson cutis gyrata syndrome
  6. Bladder carcinoma
  7. Bladder papillary transitional cell neop
  8. Bladder transitional cell papilloma
  9. Bone development disease
  10. Bone disease
  11. Bone marrow cancer
  12. Bone marrow disease
  13. Brachydactyly
  14. Cancer
  15. Carcinoma
  16. Cardiovascular system disease
  17. Cell type cancer
  18. Choanal atresia
  19. Craniosynostosis
  20. Crouzon syndrome
  21. Dermatitis
  22. Dermatosis papulosa nigra
  23. Disease
  24. Disease of anatomical entity
  25. Disease of cellular proliferation
  26. Dysostosis
  27. Exophthalmos
  28. Genetic disease
  29. Genitourinary cancer
  30. Hematologic cancer
  31. Hematopoietic system disease
  32. Hydrocephalus
  33. Hypertropia
  34. Hypochondroplasia
  35. Integumentary system disease
  36. Intracranial hypertension
  37. Keratosis
  38. LADD syndrome
  39. Leukemia
  40. Lymphoid leukemia
  41. Mature B-cell lymphocytic neoplasm
  42. Medical disorder
  43. Monoclonal gammopathy of uncertain signi
  44. Monogenic disease
  45. Multiple myeloma
  46. Musculoskeletal system disease
  47. Myeloma
  48. Organ system cancer
  49. Osteochondrodysplasia
  50. Osteogenesis imperfecta
  51. Pfeiffer syndrome
  52. Physical disorder
  53. Plasma cell neoplasm
  54. Saethre-Chotzen syndrome
  55. Seborrheic keratosis
  56. Sensorineural hearing loss
  57. Skin disease
  58. Smoldering myeloma
  59. Spondyloepimetaphyseal dysplasia
  60. Spondyloepiphyseal dysplasia congenita
  61. Syndactyly
  62. Synostosis
  63. Thanatophoric dysplasia
  64. Urinary bladder cancer
  65. Urinary tract cancer
  66. Urinary tract neoplasm
  67. Urinary tract papillary transitional cel
  68. Wolf-Hirschhorn syndrome

Stage Associations

This gene is associated with the following stages: No Stages were found