Gene Expression: SHH

Gene Data

  • Gene Symbol: SHH
  • Gene ID: 6469
  • Synonyms: HHG1, HLP3, HPE3, MCOPCB5, SMMCI, TPT, TPTPS
  • Description: sonic hedgehog
  • Database Refs: HGNC:10848, MIM:600725, HPRD:02838
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 7 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 106 diseases, scroll to view all:
  1. Acheiropody
  2. Acrocephalosyndactylia
  3. Adult central nervous system primitive n
  4. Adult medulloblastoma
  5. alcohol-related birth defect
  6. alcohol-related neurodevelopmental disor
  7. Atrophic gastritis
  8. Bardet-Biedl syndrome
  9. Basal cell carcinoma
  10. Basal ganglia disease
  11. Bone development disease
  12. Bone disease
  13. Brachydactyly
  14. Brain cancer
  15. Brain disease
  16. Brain neoplasm
  17. Cancer
  18. Carcinoma
  19. Cell type cancer
  20. Central nervous system cancer
  21. Central nervous system disease
  22. Central nervous system neoplasm
  23. Childhood brain tumor
  24. Childhood central nervous system primiti
  25. Childhood malignant central nervous syst
  26. Childhood medulloblastoma
  27. Choanal atresia
  28. Cleft lip
  29. Cleft palate
  30. Coloboma
  31. Complex genetic disease
  32. Congenital diaphragmatic hernia
  33. Congenital nervous system abnormality
  34. Craniosynostosis
  35. Desmoplastic medulloblastoma
  36. Developmental disease of mental health
  37. Disease
  38. Disease of anatomical entity
  39. Disease of cellular proliferation
  40. Dysostosis
  41. Embryonal cancer
  42. Embryonal cancer of CNS
  43. Endocrine gland cancer
  44. Esophageal atresia
  45. Esophageal disease
  46. Fetal alcohol syndrome
  47. Gastric squamous cell carcinoma
  48. Gastric tubular adenocarcinoma
  49. Gastritis
  50. Gastrointestinal system cancer
  51. Gastrointestinal system disease
  52. Genetic disease
  53. Genitourinary cancer
  54. Germ cell and embryonal cancer
  55. Germ cell cancer
  56. Glioma
  57. Greig cephalopolysyndactyly syndrome
  58. Holoprosencephaly
  59. Hydronephrosis
  60. Hypospadias
  61. Imperforate anus
  62. Inborn errors lipid metabolism
  63. Intellectual disability
  64. Intracranial neoplasm
  65. Male reproductive organ cancer
  66. Malignant glioma
  67. Malignant intracranial neoplasm
  68. Medical disorder
  69. Medulloblastoma
  70. Microcephaly
  71. Microphthalmia
  72. Monogenic disease
  73. Musculoskeletal system disease
  74. Nervous system cancer
  75. Nervous system disease
  76. Neurodegenerative disease
  77. Neuroectodermal tumor
  78. Nevoid basal cell carcinoma syndrome
  79. Organ system cancer
  80. Orofacial cleft
  81. Pallister-Hall syndrome
  82. Pancreas adenocarcinoma
  83. Pancreatic cancer
  84. Pancreatic carcinoma
  85. Pancreatic ductal adenocarcinoma
  86. Parkinson's disease
  87. Partial fetal alcohol syndrome
  88. Patau syndrome
  89. Pediatric central nervous system tumor
  90. Physical disorder
  91. Polydactyly
  92. Primitive neuroectodermal tumor
  93. Prostate cancer
  94. Reproductive organ cancer
  95. Situs inversus
  96. Skin cancer
  97. Skin carcinoma
  98. Smith-Lemli-Opitz syndrome
  99. Specific developmental disease
  100. Spina bifida
  101. Stomach disease
  102. Syndactyly
  103. Syndrome
  104. Synostosis
  105. VACTERL association
  106. Visceral heterotaxy

Stage Associations

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