Gene Expression: PYGM

Gene Data

  • Gene Symbol: PYGM
  • Gene ID: 5837
  • Synonyms: -
  • Description: phosphorylase, glycogen, muscle
  • Database Refs: HGNC:9726, MIM:608455, Ensembl:ENSG00000068976, HPRD:01986, Vega:OTTHUMG00000066835
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 21 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. Acute myocardial infarction
  2. Adenoma
  3. Adenosine deaminase deficiency
  4. Benign neoplasm
  5. Cancer
  6. Carbohydrate metabolism disease
  7. Carcinoma
  8. Cardiovascular system disease
  9. Cell type cancer
  10. Central core myopathy
  11. Cutaneous adenocystic carcinoma
  12. cytochrome-c oxidase deficiency
  13. Diabetes mellitus
  14. Disease
  15. Disease of anatomical entity
  16. Disease of cellular proliferation
  17. Disease of metabolism
  18. Endocrine pancreas disease
  19. Endocrine syndrome
  20. Endocrine system disease
  21. Extrinsic cardiomyopathy
  22. fructose-1,6-bisphosphatase deficiency
  23. Gastrointestinal system cancer
  24. Gastrointestinal system disease
  25. Genetic disease
  26. Glucose metabolism disease
  27. Glycogen storage disease
  28. Glycogen storage disease II
  29. Glycogen storage disease III
  30. Glycogen storage disease IV
  31. Glycogen storage disease IX
  32. Glycogen storage disease V
  33. Glycogen storage disease VI
  34. Glycogen storage disease VIII
  35. Heart disease
  36. Hepatobiliary disease
  37. Hyperglycemia
  38. Hyperinsulinism
  39. Hypoglycemia
  40. Inborn errors carbohydrate metabolism
  41. Inborn errors fructose metabolism
  42. Inborn errors of metabolism
  43. Intermediate coronary syndrome
  44. Ischemia
  45. Lactic acidosis
  46. Liver cirrhosis
  47. Lysosomal storage disease
  48. Malignant hyperthermia
  49. Mitochondrial disease
  50. Mitochondrial myopathy
  51. Monogenic disease
  52. Multiple endocrine neoplasia
  53. Muscle tissue disease
  54. Muscular disease
  55. Musculoskeletal system disease
  56. Myocardial infarction
  57. Myocardial ischemia
  58. Myopathy
  59. Nervous system disease
  60. Neuromuscular disease
  61. Neuropathy
  62. Organ system cancer
  63. Pancreas disease
  64. Purine nucleoside phosphorylase deficien
  65. Sweat gland carcinoma
  66. Transverse colon cancer
  67. Vascular disease
  68. Wermer syndrome

Stage Associations

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