Gene Expression: IKBKG

Gene Data

  • Gene Symbol: IKBKG
  • Gene ID: 8517
  • Synonyms: AMCBX1, FIP-3, FIP3, Fip3p, IKK-gamma, IP, IP1, IP2, IPD2, NEMO, ZC2HC9
  • Description: inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
  • Database Refs: HGNC:5961, MIM:300248, Ensembl:ENSG00000073009, HPRD:02217, Vega:OTTHUMG00000024234
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 13 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 80 diseases, scroll to view all:
  1. Aicardi syndrome
  2. Alopecia
  3. Anhidrosis
  4. Birt-Hogg-Dube syndrome
  5. Bloch-Sulzberger syndrome
  6. Brain disease
  7. Cardiovascular system disease
  8. Central nervous system disease
  9. Central retinal artery occlusion
  10. Coats disease
  11. Complex genetic disease
  12. Congenital syphilis
  13. Cortical blindness
  14. Cranial nerve disease
  15. Cystic lymphangioma
  16. Dermatitis
  17. Developmental disease of mental health
  18. Disease
  19. Disease of anatomical entity
  20. Dysgammaglobulinemia
  21. Dyskeratosis congenita
  22. Eosinophilia
  23. Erythropoietic porphyria
  24. Exudative vitreoretinopathy
  25. Eye and adnexa disease
  26. Eye degenerative disease
  27. Eye disease
  28. Facial hemiatrophy
  29. Familial atypical multiple mole-melanoma
  30. Focal dermal hypoplasia
  31. Genetic disease
  32. Genetic skin disease
  33. Globe disease
  34. Hair disease
  35. Hypohidrotic ectodermal dysplasia
  36. Hypotrichosis
  37. Incontinentia pigmenti achromians
  38. Integumentary system disease
  39. Intellectual disability
  40. Keratoacanthoma
  41. Larsen syndrome
  42. Lennox-Gastaut syndrome
  43. Letterer-Siwe disease
  44. Leukocoria
  45. Leukocyte disease
  46. Lichen nitidus
  47. Lymphangioma
  48. Lymphatic system disease
  49. Lymphedema
  50. Medical disorder
  51. Microcephaly
  52. Microphthalmia
  53. Mongolian spot
  54. Monogenic disease
  55. Nervous system disease
  56. Neurofibromatosis
  57. Optic atrophy
  58. Orbital cyst
  59. Osteopetrosis
  60. Osteosclerosis
  61. Physical disorder
  62. Pigmentation disease
  63. Proteus syndrome
  64. Retinal artery occlusion
  65. Retinal detachment
  66. Retinal disease
  67. Retinal perforation
  68. Retinal telangiectasia
  69. Retinopathy of prematurity
  70. Selective immunoglobulin deficiency dise
  71. Sensory system disease
  72. Skin disease
  73. Skin squamous cell carcinoma
  74. Specific developmental disease
  75. Spongiotic dermatitis
  76. Sweat gland disease
  77. Tuberous sclerosis
  78. Urticaria pigmentosa
  79. Visual cortex disease
  80. Visual pathway disease

Stage Associations

This gene is associated with the following stages: