History:GENE:DLK1    

Gene Expression: NR0B1

Gene Data

  • Gene Symbol: NR0B1
  • Gene ID: 190
  • Synonyms: AHC, AHCH, AHX, DAX-1, DAX1, DSS, GTD, HHG, NROB1, SRXY2
  • Description: nuclear receptor subfamily 0, group B, member 1
  • Database Refs: HGNC:7960, MIM:300473, HPRD:08362
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 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 70 diseases, scroll to view all:
  1. Acrocallosal syndrome
  2. Acute hemorrhagic conjunctivitis
  3. Addison's disease
  4. Adenoma
  5. Adrenal cancer
  6. Adrenal carcinoma
  7. Adrenal cortical hypofunction
  8. Adrenal gland cancer
  9. Adrenal gland disease
  10. Adrenal hyperplasia
  11. Aland Island eye disease
  12. Alternating hemiplegia of childhood
  13. Amenorrhea
  14. Atrophic muscular disease
  15. Benign neoplasm
  16. Bone development disease
  17. Botulism
  18. Brain disease
  19. Campomelic dysplasia
  20. Cancer
  21. Cell type cancer
  22. Central nervous system disease
  23. Choriocarcinoma
  24. Chromosomal disease
  25. Delayed puberty
  26. Developmental disease of mental health
  27. Disease
  28. Disease of anatomical entity
  29. Disease of cellular proliferation
  30. Duchenne muscular dystrophy
  31. Endocrine system disease
  32. Epilepsy
  33. Genetic disease
  34. Genitourinary cancer
  35. Germ cell and embryonal cancer
  36. Germ cell cancer
  37. Gestational trophoblastic neoplasm
  38. Gonadal disease
  39. Gonadal dysgenesis
  40. Hemiplegia
  41. Hypogonadism
  42. Infertility
  43. Intellectual disability
  44. Kallmann syndrome
  45. Klinefelter's syndrome
  46. Metaphyseal dysplasia
  47. Migraine
  48. Monogenic disease
  49. Muscle tissue disease
  50. Muscular disease
  51. Muscular dystrophy
  52. Musculoskeletal system disease
  53. Myopathy
  54. Nephroblastoma
  55. Nervous system disease
  56. Neuromuscular disease
  57. Neuropathy
  58. Organ system cancer
  59. Osteochondrodysplasia
  60. Panophthalmitis
  61. Placenta neoplasm
  62. Placental site trophoblastic tumor
  63. Precocious puberty
  64. Punctate epithelial keratoconjunctivitis
  65. Purulent endophthalmitis
  66. Pyosalpinx
  67. red-green color blindness
  68. Reproductive system disease
  69. Specific developmental disease
  70. Trophoblastic neoplasm

Stage Associations

This gene is associated with the following stages: