Gene Expression: MNX1

Gene Data

  • Gene Symbol: MNX1
  • Gene ID: 3110
  • Synonyms: HB9, HLXB9, HOXHB9, SCRA1
  • Description: motor neuron and pancreas homeobox 1
  • Database Refs: HGNC:4979, MIM:142994, Ensembl:ENSG00000130675, HPRD:00874, Vega:OTTHUMG00000157181
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 2 out of 6 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 80 diseases, scroll to view all:
  1. Acute leukemia
  2. Acute myeloid leukemia
  3. Adenocarcinoma
  4. Anemia
  5. Aniridia
  6. Anterior horn cell disease
  7. Autism
  8. Autism spectrum disease
  9. Baller-Gerold syndrome
  10. Bone development disease
  11. Bowel dysfunction
  12. Branchiootorenal syndrome
  13. Cancer
  14. Carcinoma
  15. Cardiovascular system disease
  16. Cell type cancer
  17. Central nervous system hereditary degene
  18. Cleft lip
  19. Cleft palate
  20. Coloboma
  21. Colonic disease
  22. Complex genetic disease
  23. cone-rod dystrophy
  24. Congenital nervous system abnormality
  25. Constipation
  26. Craniosynostosis
  27. Developmental disease of mental health
  28. Disease
  29. Disease of anatomical entity
  30. Disease of cellular proliferation
  31. Disease of mental health
  32. Dyskinetic cerebral palsy
  33. Dysostosis
  34. Embryonal cancer
  35. Embryonal carcinoma
  36. Eye and adnexa disease
  37. Eye disease
  38. Facioscapulohumeral muscular dystrophy
  39. Gastrointestinal system disease
  40. Genetic disease
  41. Genitourinary cancer
  42. Germ cell and embryonal cancer
  43. Germ cell cancer
  44. Globe disease
  45. Hematologic cancer
  46. Hematopoietic system disease
  47. Holoprosencephaly
  48. Intellectual disability
  49. Keratoconus
  50. Leukemia
  51. Lymphoblastic leukemia
  52. Male reproductive organ cancer
  53. Medical disorder
  54. Megacolon
  55. Meningocele
  56. Microphthalmia
  57. Motor neuron disease
  58. Muscle tissue disease
  59. Muscular disease
  60. Musculoskeletal system disease
  61. Myeloid leukemia
  62. Myopathy
  63. Nervous system disease
  64. Neuromuscular disease
  65. Neuropathy
  66. Organ system cancer
  67. Orofacial cleft
  68. Pancytopenia
  69. Pervasive developmental disease
  70. Physical disorder
  71. Pituitary hypoplasia
  72. Polydactyly
  73. Prostate cancer
  74. Reproductive organ cancer
  75. Sensory system disease
  76. Specific developmental disease
  77. Spina bifida
  78. Synostosis
  79. Teratoma
  80. Tooth agenesis

Stage Associations

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