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Gene Expression: MMD

Gene Data

  • Gene Symbol: MMD
  • Gene ID: 23531
  • Synonyms: MMA, MMD1, PAQR11
  • Description: monocyte to macrophage differentiation-associated
  • Database Refs: HGNC:7153, MIM:604467, Ensembl:ENSG00000108960, HPRD:06835, Vega:OTTHUMG00000177845
  • 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:

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 64 diseases, scroll to view all:
  1. Anemia
  2. Argininosuccinic aciduria
  3. Brain disease
  4. Breast disease
  5. Cancer
  6. Carbohydrate metabolism disease
  7. Cardiovascular system disease
  8. Central core myopathy
  9. Central nervous system disease
  10. Cerebral arterial disease
  11. Cerebrovascular accident
  12. Cerebrovascular disease
  13. Congenital structural myopathy
  14. Disease
  15. Disease of anatomical entity
  16. Disease of cellular proliferation
  17. Disease of metabolism
  18. Endocrine pancreas disease
  19. Endocrine system disease
  20. Female stress incontinence
  21. Gastrointestinal system disease
  22. Genetic disease
  23. Glucose metabolism disease
  24. Hartnup disease
  25. Hemopneumothorax
  26. Homocystinuria
  27. Hyperhomocysteinemia
  28. Inborn errors of amino acid metabolism
  29. Inborn errors of metabolism
  30. Inborn metabolic brain disease
  31. Intracranial arterial disease
  32. Ischemia
  33. Isovaleric acidemia
  34. Kidney disease
  35. Kidney failure
  36. Macrocytic anemia
  37. Malignant hyperthermia
  38. Maple syrup urine disease
  39. Mastitis
  40. Megaloblastic anemia
  41. Metabolic brain disease
  42. Methylmalonic aciduria
  43. Monogenic disease
  44. Moyamoya disease
  45. Multiple carboxylase deficiency
  46. Musculoskeletal system disease
  47. Nervous system disease
  48. Neuropathy
  49. Nutrition disease
  50. Nutritional deficiency disease
  51. Organ system cancer
  52. Ornithine carbamoyltransferase deficienc
  53. Pancreas disease
  54. Peripheral nervous system disease
  55. Peripheral neuropathy
  56. Phaeohyphomycosis
  57. Phenylketonuria
  58. Propionic acidemia
  59. Skull base meningioma
  60. Sulfuraminoacidemia
  61. Transient cerebral ischemia
  62. Tyrosinemia
  63. Urinary system disease
  64. Vascular disease

Stage Associations

This gene is associated with the following stages: