History:GENE:MUC3A    GENE:S100A4    

Gene Expression: MECOM

Gene Data

  • Gene Symbol: MECOM
  • Gene ID: 2122
  • Synonyms: AML1-EVI-1, EVI1, MDS1, MDS1-EVI1, PRDM3
  • Description: MDS1 and EVI1 complex locus
  • Database Refs: HGNC:3498, MIM:165215, Ensembl:ENSG00000085276, HPRD:01310, Vega:OTTHUMG00000158596
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 26 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 80 diseases, scroll to view all:
  1. Acrocephalosyndactylia
  2. Acrocephalosyndactylia
  3. Acute myeloid leukemia
  4. Acute myeloid leukemia
  5. Basal cell carcinoma
  6. Basal cell carcinoma
  7. Bone development disease
  8. Bone development disease
  9. Borjeson-Forssman-Lehmann syndrome
  10. Borjeson-Forssman-Lehmann syndrome
  11. Cancer
  12. Cancer
  13. Cardiovascular system disease
  14. Cardiovascular system disease
  15. Cell type cancer
  16. Cell type cancer
  17. Charcot-Marie-Tooth disease type 1
  18. Charcot-Marie-Tooth disease type 1
  19. Charcot-Marie-Tooth disease type 3
  20. Charcot-Marie-Tooth disease type 3
  21. Congenital heart defect
  22. Congenital heart defect
  23. Denys-Drash syndrome
  24. Denys-Drash syndrome
  25. Disease
  26. Disease
  27. Disease of anatomical entity
  28. Disease of anatomical entity
  29. Disease of cellular proliferation
  30. Disease of cellular proliferation
  31. Dysostosis
  32. Dysostosis
  33. Frasier syndrome
  34. Frasier syndrome
  35. Genitourinary cancer
  36. Genitourinary cancer
  37. Goldenhar syndrome
  38. Goldenhar syndrome
  39. Gonadoblastoma
  40. Gonadoblastoma
  41. Greig cephalopolysyndactyly syndrome
  42. Greig cephalopolysyndactyly syndrome
  43. Heart septal defect
  44. Heart septal defect
  45. Hematologic cancer
  46. Hematologic cancer
  47. Imperforate anus
  48. Imperforate anus
  49. Kidney cancer
  50. Kidney cancer
  51. Leukemia
  52. Leukemia
  53. Medical disorder
  54. Medical disorder
  55. Myeloid leukemia
  56. Myeloid leukemia
  57. Nephroblastoma
  58. Nephroblastoma
  59. Organ system cancer
  60. Organ system cancer
  61. Pallister-Hall syndrome
  62. Pallister-Hall syndrome
  63. Physical disorder
  64. Physical disorder
  65. Piebaldism
  66. Piebaldism
  67. Polydactyly
  68. Polydactyly
  69. Pulmonary valve disease
  70. Pulmonary valve disease
  71. Pulmonary valve stenosis
  72. Pulmonary valve stenosis
  73. Synostosis
  74. Synostosis
  75. Urinary tract cancer
  76. Urinary tract cancer
  77. Ventricular septal defect
  78. Ventricular septal defect
  79. Waardenburg's syndrome
  80. Waardenburg's syndrome

Stage Associations

This gene is associated with the following stages: