History:GENE:GTF2B    GENE:CCRN4L    

Gene Expression: CBS

Gene Data

  • Gene Symbol: CBS
  • Gene ID: 875
  • Synonyms: HIP4
  • Description: cystathionine-beta-synthase
  • Database Refs: HGNC:1550, MIM:613381, Ensembl:ENSG00000160200, HPRD:01994, Vega:OTTHUMG00000086834
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 22 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 76 diseases, scroll to view all:
  1. Alzheimer's disease
  2. Aphasia
  3. Apraxia
  4. Arterial occlusive disease
  5. Arteriopathy
  6. Arteriosclerosis
  7. Arteriosclerotic cardiovascular disease
  8. Asymmetric motor neuropathy
  9. Atherosclerosis
  10. Basal ganglia disease
  11. Brain disease
  12. Cancer
  13. Cardiovascular system disease
  14. Central nervous system disease
  15. Cerebrovascular accident
  16. Cerebrovascular disease
  17. Chromosomal disease
  18. Cicatricial ectropion
  19. Cognitive disease
  20. Communication disease
  21. Dementia
  22. Developmental disease of mental health
  23. Disease
  24. Disease of anatomical entity
  25. Disease of cellular proliferation
  26. Disease of mental health
  27. Disease of metabolism
  28. Down syndrome
  29. Extrinsic cardiomyopathy
  30. Fetishism
  31. Frontotemporal dementia
  32. Fungal infectious disease
  33. Gait apraxia
  34. Gastrointestinal system disease
  35. Genetic disease
  36. Gitelman syndrome
  37. Heart disease
  38. Homocystinuria
  39. Hyperhomocysteinemia
  40. Hypermethioninemia
  41. Hypertension
  42. Ideomotor apraxia
  43. Inborn errors of amino acid metabolism
  44. Inborn errors of metabolism
  45. Inborn metabolic brain disease
  46. Intellectual disability
  47. Intracranial thrombosis
  48. Ischemia
  49. Language disease
  50. Medical disorder
  51. Metabolic brain disease
  52. Monogenic disease
  53. Movement disease
  54. Multiple system atrophy
  55. Muscle tissue disease
  56. Muscular disease
  57. Musculoskeletal system disease
  58. Myocardial ischemia
  59. Myopathy
  60. Nervous system disease
  61. Neurodegenerative disease
  62. Organ system cancer
  63. Pityriasis versicolor
  64. Progressive supranuclear palsy
  65. Psychomotor disease
  66. Specific developmental disease
  67. Spina bifida
  68. Sulfuraminoacidemia
  69. Superficial mycosis
  70. Tauopathy
  71. Tinea corporis
  72. Tinea manuum
  73. Transvestism
  74. Trichosporonosis
  75. Vascular disease
  76. Voyeurism

Stage Associations

This gene is associated with the following stages: