Gene Expression: FGFR1

Gene Data

  • Gene Symbol: FGFR1
  • Gene ID: 2260
  • Synonyms: BFGFR, CD331, CEK, FGFBR, FGFR-1, FLG, FLT-2, FLT2, HBGFR, HH2, HRTFDS, KAL2, N-SAM, OGD, bFGF-R-1
  • Description: fibroblast growth factor receptor 1
  • Database Refs: HGNC:3688, MIM:136350, Ensembl:ENSG00000077782, HPRD:00634, Vega:OTTHUMG00000147366
  • 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 89 diseases, scroll to view all:
  1. Achondroplasia
  2. Acrocephalosyndactylia
  3. Acute leukemia
  4. Acute myeloid leukemia
  5. Adenocarcinoma
  6. Astrocytoma
  7. Bone development disease
  8. Bone disease
  9. Bone marrow cancer
  10. Bone marrow disease
  11. Brain cancer
  12. Brain neoplasm
  13. Breast cancer
  14. Cancer
  15. Carcinoma
  16. Cardiovascular system disease
  17. Cell type cancer
  18. Central nervous system cancer
  19. Central nervous system neoplasm
  20. Chromosomal disease
  21. Chronic myeloid leukemia
  22. Cleft lip
  23. Cleft palate
  24. Connective tissue neoplasm
  25. Craniosynostosis
  26. Crouzon syndrome
  27. Cryptorchidism
  28. Delayed puberty
  29. Disease
  30. Disease of anatomical entity
  31. Disease of cellular proliferation
  32. Dysostosis
  33. Endocrine system disease
  34. Eosinophilia
  35. Gastrointestinal system cancer
  36. Genetic disease
  37. Genitourinary cancer
  38. Glioblastoma
  39. Gonadal disease
  40. Hematologic cancer
  41. Hematopoietic system disease
  42. Hypochondroplasia
  43. Hypogonadism
  44. Hypophosphatemia
  45. Intracranial neoplasm
  46. Juvenile myelomonocytic leukemia
  47. Kallmann syndrome
  48. Klinefelter's syndrome
  49. Leukemia
  50. Leukocyte disease
  51. Lung cancer
  52. Lymphoma
  53. Male reproductive organ cancer
  54. Malignant intracranial neoplasm
  55. Mastocytosis
  56. Medical disorder
  57. Mesenchymal cell neoplasm
  58. Monogenic disease
  59. Musculoskeletal system disease
  60. Myelodysplastic myeloproliferative cance
  61. Myelofibrosis
  62. Myeloid leukemia
  63. Myeloma
  64. Nervous system cancer
  65. Nervous system disease
  66. Organ system cancer
  67. Orofacial cleft
  68. Osteochondrodysplasia
  69. Pfeiffer syndrome
  70. Phosphorus metabolism disease
  71. Physical disorder
  72. Polycythemia
  73. Polycythemia vera
  74. Prostate cancer
  75. Radioulnar synostosis
  76. Renal agenesis
  77. Reproductive organ cancer
  78. Reproductive system disease
  79. Respiratory system cancer
  80. Saethre-Chotzen syndrome
  81. Sensory system disease
  82. Soft tissue cancer
  83. Stem cell leukemia
  84. Syndactyly
  85. Synostosis
  86. Systemic mastocytosis
  87. Thanatophoric dysplasia
  88. Thoracic cancer
  89. Thrombocytosis

Stage Associations

This gene is associated with the following stages: