Gene Expression: FMR1

Gene Data

  • Gene Symbol: FMR1
  • Gene ID: 2332
  • Synonyms: FMRP, FRAXA, POF, POF1
  • Description: fragile X mental retardation 1
  • Database Refs: HGNC:3775, MIM:309550, Ensembl:ENSG00000102081, HPRD:02398, Vega:OTTHUMG00000022606
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 1 out of 23 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 36 diseases, scroll to view all:
  1. Attention deficit hyperactivity disease
  2. Autism
  3. Autism spectrum disease
  4. Central nervous system disease
  5. Chromosomal disease
  6. Developmental disease of mental health
  7. Disease
  8. Disease of anatomical entity
  9. Disease of mental health
  10. Down syndrome
  11. Essential tremor
  12. Female reproductive system disease
  13. Fragile X syndrome
  14. Genetic disease
  15. Infertility
  16. Intellectual disability
  17. Learning disability
  18. Monogenic disease
  19. Myotonic disease
  20. Myotonic dystrophy
  21. Nervous system disease
  22. Neurodegenerative disease
  23. Ovarian disease
  24. Ovarian dysfunction
  25. Peripheral nervous system disease
  26. Peripheral neuropathy
  27. Pervasive developmental disease
  28. Prader-Willi syndrome
  29. Premature menopause
  30. Premature ovarian failure
  31. Reproductive system disease
  32. Rett syndrome
  33. Specific developmental disease
  34. Specific phobia
  35. Spinocerebellar ataxia
  36. Spinocerebellar degeneration

Stage Associations

This gene is associated with the following stages: