History:GENE:RELN    

Gene Expression: MECP2

Gene Data

  • Gene Symbol: MECP2
  • Gene ID: 4204
  • Synonyms: AUTSX3, MRX16, MRX79, MRXS13, MRXSL, PPMX, RS, RTS, RTT
  • Description: methyl CpG binding protein 2 (Rett syndrome)
  • Database Refs: HGNC:6990, MIM:300005, Ensembl:ENSG00000169057, HPRD:02050, Vega:OTTHUMG00000024229
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 3 out of 4 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 29 diseases, scroll to view all:
  1. Angelman syndrome
  2. Apraxia
  3. Autism
  4. Autism spectrum disease
  5. Brain disease
  6. Central nervous system disease
  7. Chromosomal disease
  8. Congenital nervous system abnormality
  9. Developmental disease of mental health
  10. Disease
  11. Disease of anatomical entity
  12. Disease of mental health
  13. Down syndrome
  14. Fragile X syndrome
  15. Gait apraxia
  16. Genetic disease
  17. Intellectual disability
  18. Learning disability
  19. Medical disorder
  20. Microcephaly
  21. Monogenic disease
  22. Nervous system disease
  23. Pervasive developmental disease
  24. Physical disorder
  25. Prader-Willi syndrome
  26. Psychomotor disease
  27. Rett syndrome
  28. Rubinstein-Taybi syndrome
  29. Specific developmental disease

Stage Associations

This gene is associated with the following stages: