History:GENE:EXT1    GENE:TRH    

Gene Expression: PTCH1

Gene Data

  • Gene Symbol: PTCH1
  • Gene ID: 5727
  • Synonyms: BCNS, HPE7, NBCCS, PTC, PTC1, PTCH, PTCH11
  • Description: patched 1
  • Database Refs: HGNC:9585, MIM:601309, Ensembl:ENSG00000185920, HPRD:03200, Vega:OTTHUMG00000020280
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 2 out of 33 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 91 diseases, scroll to view all:
  1. Accommodative esotropia
  2. Amblyopia
  3. Ametropic amblyopia
  4. Anisometropia
  5. Atrial heart septal defect
  6. Basal cell carcinoma
  7. Bone development disease
  8. Brachydactyly
  9. Brain disease
  10. Brain neoplasm
  11. Brown-Sequard syndrome
  12. Cancer
  13. Carcinoma
  14. Carotid stenosis
  15. Cell type cancer
  16. Central nervous system cancer
  17. Central nervous system disease
  18. Central nervous system neoplasm
  19. Childhood brain tumor
  20. Cleft lip
  21. Congenital heart defect
  22. Congenital nervous system abnormality
  23. Corneal disease
  24. Corneal edema
  25. Desmoplastic medulloblastoma
  26. Disease
  27. Disease of anatomical entity
  28. Disease of cellular proliferation
  29. Disuse ambylopia
  30. Dysostosis
  31. Embryonal cancer
  32. Embryonal cancer of CNS
  33. Embryonal rhabdomyosarcoma
  34. Endocrine gland cancer
  35. Esotropia
  36. Eye and adnexa disease
  37. Eye disease
  38. Genetic disease
  39. Germ cell and embryonal cancer
  40. Germ cell cancer
  41. Glioma
  42. Globe disease
  43. Greig cephalopolysyndactyly syndrome
  44. Heart septal defect
  45. Holoprosencephaly
  46. Hyperopia
  47. Inferior vena cava leiomyosarcoma
  48. Inferior vena cava malignant neoplasm
  49. Intracranial neoplasm
  50. Malignant glioma
  51. Medical disorder
  52. Medulloblastoma
  53. Mesenchymal cell neoplasm
  54. Monogenic disease
  55. Muscle cancer
  56. Nervous system cancer
  57. Nervous system disease
  58. Neuroectodermal tumor
  59. Nevoid basal cell carcinoma syndrome
  60. Nodular medulloblastoma
  61. Ocular motility disease
  62. Organ system cancer
  63. Pallister-Hall syndrome
  64. Pancreatic cancer
  65. Papillary carcinoma
  66. Papillary thyroid carcinoma
  67. Paralytic squint
  68. Partial third-nerve palsy
  69. Physical disorder
  70. Polydactyly
  71. Primitive neuroectodermal tumor
  72. Pulmonary valve insufficiency
  73. Refractive error
  74. Rhabdomyosarcoma
  75. Sensory system disease
  76. Short bowel syndrome
  77. Sipple syndrome
  78. Skeletal muscle cancer
  79. Skin cancer
  80. Skin carcinoma
  81. Smith-Lemli-Opitz syndrome
  82. Soft tissue cancer
  83. Strabismus
  84. Suppression amblyopia
  85. Synostosis
  86. Thyroid cancer
  87. Thyroid carcinoma
  88. Thyroid neoplasm
  89. Transient cerebral ischemia
  90. Ventricular septal defect
  91. Xeroderma pigmentosum

Stage Associations

This gene is associated with the following stages: