History:GENE:CYP11A1    

Gene Expression: TGM2

Gene Data

  • Gene Symbol: TGM2
  • Gene ID: 7052
  • Synonyms: G-ALPHA-h, GNAH, TG2, TGC
  • Description: transglutaminase 2
  • Database Refs: HGNC:11778, MIM:190196, Ensembl:ENSG00000198959, HPRD:01825, Vega:OTTHUMG00000032437
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 1 out of 18 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 69 diseases, scroll to view all:
  1. Addison's disease
  2. Adrenal cortical hypofunction
  3. Alzheimer's disease
  4. Anemia
  5. Autoimmune disease of endocrine system
  6. Autoimmune disease of gastrointestinal t
  7. Autoimmune disease of skin and connectiv
  8. Autoimmune disease of urogenital tract
  9. Autoimmune hepatitis
  10. Autoimmune thyroiditis
  11. B cell deficiency
  12. Bone disease
  13. Bone remodeling disease
  14. Bone resorption disease
  15. Brain disease
  16. Bullous skin disease
  17. Cancer
  18. Carbohydrate metabolism disease
  19. Cardiovascular system disease
  20. Celiac disease
  21. Central nervous system disease
  22. Cognitive disease
  23. Dementia
  24. Dermatitis
  25. Dermatitis herpetiformis
  26. Diabetes mellitus
  27. Diarrhea
  28. Disease
  29. Disease of anatomical entity
  30. Disease of cellular proliferation
  31. Disease of mental health
  32. Disease of metabolism
  33. Endocrine pancreas disease
  34. Endocrine system disease
  35. Gastrointestinal system disease
  36. Glucose metabolism disease
  37. Hematopoietic system disease
  38. Hepatobiliary disease
  39. Huntington's disease
  40. Hypersensitivity reaction disease
  41. Hypersensitivity reaction type II diseas
  42. Immune system disease
  43. Immunoglobulin alpha deficiency
  44. Inflammatory bowel disease
  45. Integumentary system disease
  46. Intestinal disease
  47. Iron deficiency anemia
  48. Irritable bowel syndrome
  49. Liver cirrhosis
  50. Liver disease
  51. Lymphocytic gastritis
  52. Microcytic anemia
  53. Musculoskeletal system disease
  54. Nervous system disease
  55. Neuroblastoma
  56. Neurodegenerative disease
  57. Nutrition disease
  58. Nutritional deficiency disease
  59. Organ system cancer
  60. Osteoporosis
  61. Pancreas disease
  62. Primary biliary cirrhosis
  63. Primary immunodeficiency disease
  64. Skin disease
  65. Stomach disease
  66. Syndrome
  67. Tauopathy
  68. Thyroid gland disease
  69. Thyroiditis

Stage Associations

This gene is associated with the following stages: