Gene Expression: NPTX2

Gene Data

  • Gene Symbol: NPTX2
  • Gene ID: 4885
  • Synonyms: NARP, NP-II, NP2
  • Description: neuronal pentraxin II
  • Database Refs: HGNC:7953, MIM:600750, Ensembl:ENSG00000106236, HPRD:02853, Vega:OTTHUMG00000154369
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 1 out of 5 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 44 diseases, scroll to view all:
  1. Brain disease
  2. Central nervous system disease
  3. Cerebellar disease
  4. Cerebrovascular accident
  5. Cerebrovascular disease
  6. Chronic progressive external ophthalmopl
  7. Cranial nerve disease
  8. Diabetes insipidus
  9. Disease
  10. Disease of anatomical entity
  11. Disease of metabolism
  12. Endocrine system disease
  13. Eye and adnexa disease
  14. Eye disease
  15. Globe disease
  16. Hypertrophic cardiomyopathy
  17. Inborn errors of metabolism
  18. Inborn metabolic brain disease
  19. Kearns-Sayre syndrome
  20. Lactic acidosis
  21. Leber hereditary optic neuropathy
  22. Leigh disease
  23. MELAS syndrome
  24. MERRF syndrome
  25. Metabolic brain disease
  26. Mitochondrial disease
  27. Mitochondrial encephalomyopathy
  28. Mitochondrial myopathy
  29. Nervous system disease
  30. Neurohypophyseal diabetes insipidus
  31. Neuropathy
  32. Ocular motility disease
  33. Ophthalmoplegia
  34. Optic nerve disease
  35. Pancreas disease
  36. Pearson syndrome
  37. Refsum disease
  38. Retinal degeneration
  39. Retinal disease
  40. Retinitis
  41. Retinitis pigmentosa
  42. Sensory system disease
  43. Visual pathway disease
  44. Wolfram syndrome

Stage Associations

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