Gene Expression: MSX2

Gene Data

  • Gene Symbol: MSX2
  • Gene ID: 4488
  • Synonyms: CRS2, FPP, HOX8, MSH, PFM, PFM1
  • Description: msh homeobox 2
  • Database Refs: HGNC:7392, MIM:123101, Ensembl:ENSG00000120149, HPRD:00421, Vega:OTTHUMG00000130556
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 2 out of 2 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 45 diseases, scroll to view all:
  1. Acrocephalosyndactylia
  2. Amelogenesis imperfecta
  3. Bone development disease
  4. Bone disease
  5. Bone remodeling disease
  6. Brachydactyly
  7. Cleft lip
  8. Cleft palate
  9. Cleidocranial dysplasia
  10. Congenital heart defect
  11. Congenital nervous system abnormality
  12. Craniometaphyseal dysplasia
  13. Craniosynostosis
  14. Dental enamel hypoplasia
  15. Dentin dysplasia
  16. Disease
  17. Disease of anatomical entity
  18. Double outlet right ventricle
  19. Dysostosis
  20. Fetal alcohol syndrome
  21. Fibrodysplasia ossificans progressiva
  22. Fibrous dysplasia
  23. Goldenhar syndrome
  24. Holoprosencephaly
  25. Inverted papilloma
  26. Medical disorder
  27. Mouth disease
  28. Musculoskeletal system disease
  29. Myositis ossificans
  30. Orofacial cleft
  31. Osteochondrodysplasia
  32. Osteopetrosis
  33. Osteosclerosis
  34. Ovarian endodermal sinus tumor
  35. Pfeiffer syndrome
  36. Physical disorder
  37. Polydactyly
  38. Saethre-Chotzen syndrome
  39. Syndactyly
  40. Synostosis
  41. Teeth hard tissue disease
  42. Tooth agenesis
  43. Tooth disease
  44. Treacher Collins syndrome
  45. Ventricular septal defect

Stage Associations

This gene is associated with the following stages: