Gene Expression: MSX1

Gene Data

  • Gene Symbol: MSX1
  • Gene ID: 4487
  • Synonyms: ECTD3, HOX7, HYD1, STHAG1
  • Description: msh homeobox 1
  • Database Refs: HGNC:7391, MIM:142983, Ensembl:ENSG00000163132, HPRD:00866, Vega:OTTHUMG00000090335
  • 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 33 diseases, scroll to view all:
  1. Amelogenesis imperfecta
  2. Bamforth-Lazarus syndrome
  3. Bone development disease
  4. Bone disease
  5. Cherubism
  6. Cleft lip
  7. Cleft palate
  8. Cleidocranial dysplasia
  9. Craniometaphyseal dysplasia
  10. Craniosynostosis
  11. Dental enamel hypoplasia
  12. Dentin dysplasia
  13. Dentinogenesis imperfecta
  14. Disease
  15. Disease of anatomical entity
  16. Double outlet right ventricle
  17. Dysostosis
  18. Ellis-Van Creveld syndrome
  19. Gastrointestinal system disease
  20. Genetic disease
  21. Hypohidrotic ectodermal dysplasia
  22. Medical disorder
  23. Mouth disease
  24. Orofacial cleft
  25. Physical disorder
  26. Polydactyly
  27. Syndactyly
  28. Synostosis
  29. Tooth agenesis
  30. Tooth and nail syndrome
  31. Tooth disease
  32. Ventricular septal defect
  33. Wolf-Hirschhorn syndrome

Stage Associations

This gene is associated with the following stages: