Gene Expression: PVALB

Gene Data

  • Gene Symbol: PVALB
  • Gene ID: 5816
  • Synonyms: D22S749
  • Description: parvalbumin
  • Database Refs: HGNC:9704, MIM:168890, Ensembl:ENSG00000100362, HPRD:01353, Vega:OTTHUMG00000150547
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 6 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 73 diseases, scroll to view all:
  1. Alzheimer's disease
  2. Amyotrophic lateral sclerosis
  3. Anterior horn cell disease
  4. Autism
  5. Autism spectrum disease
  6. Bacterial infectious disease
  7. Basal ganglia disease
  8. Brain disease
  9. Brain hypoxia-Ischemia
  10. Brain ischemia
  11. Breast fibrosarcoma
  12. Cardiovascular system disease
  13. Central nervous system disease
  14. Central nervous system hereditary degene
  15. Cerebral artery occlusion
  16. Cerebrovascular disease
  17. Cholera
  18. Cognitive disease
  19. Congenital nervous system abnormality
  20. Dementia
  21. Developmental disease of mental health
  22. Disease
  23. Disease by infectious agent
  24. Disease of anatomical entity
  25. Disease of mental health
  26. Epilepsy
  27. Fetal alcohol syndrome
  28. Fibrosarcoma of soft tissue
  29. Food allergy
  30. Generalized epilepsy
  31. Huntington's disease
  32. Hypersensitivity reaction disease
  33. Hypersensitivity reaction type I disease
  34. Immune system disease
  35. Intractable epilepsy
  36. Intraocular retinoblastoma
  37. Ischemia
  38. Kidney cancer
  39. Kidney neoplasm
  40. Lissencephaly
  41. Medical disorder
  42. Motor neuron disease
  43. Muscle tissue disease
  44. Muscular disease
  45. Musculoskeletal system disease
  46. Myopathy
  47. Nervous system disease
  48. Neurodegenerative disease
  49. Neuromuscular disease
  50. Neuropathy
  51. Olivopontocerebellar atrophy
  52. Oxyphilic adenoma
  53. Parkinson's disease
  54. Pervasive developmental disease
  55. Physical disorder
  56. Primary bacterial infectious disease
  57. Prion disease
  58. Psychotic disease
  59. Renal carcinoma
  60. Renal cell carcinoma
  61. Renal oncocytoma
  62. Retinal disease
  63. Schizophrenia
  64. Scrapie
  65. Sensory system disease
  66. Tauopathy
  67. Tetanus
  68. Toxic encephalopathy
  69. Transient cerebral ischemia
  70. Urinary tract cancer
  71. Urinary tract neoplasm
  72. Vascular disease
  73. Wernicke-Korsakoff syndrome

Stage Associations

This gene is associated with the following stages: