Gene Expression: APPL1

Gene Data

  • Gene Symbol: APPL1
  • Gene ID: 26060
  • Synonyms: APPL, DIP13alpha
  • Description: adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1
  • Database Refs: HGNC:24035, MIM:604299, Ensembl:ENSG00000157500, HPRD:05053, Vega:OTTHUMG00000133756
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 24 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 63 diseases, scroll to view all:
  1. Acute contagious conjunctivitis
  2. Angelman syndrome
  3. Apraxia
  4. Atrophic muscular disease
  5. Autism
  6. Autism spectrum disease
  7. Cancer
  8. Chorioangioma
  9. Chromosomal disease
  10. Chronic kidney failure
  11. Congenital nervous system abnormality
  12. Cranial nerve disease
  13. Developmental disease of mental health
  14. Disease
  15. Disease of anatomical entity
  16. Disease of cellular proliferation
  17. Disease of mental health
  18. Duane retraction syndrome
  19. End stage renal failure
  20. Exophthalmos
  21. Eye and adnexa disease
  22. Eye disease
  23. Familial juvenile hyperuricemic nephropa
  24. Genetic disease
  25. Globe disease
  26. Hypotropia
  27. Immune system disease
  28. Imperforate anus
  29. Intellectual disability
  30. Kidney disease
  31. Kidney failure
  32. Medical disorder
  33. Microcephaly
  34. Monogenic disease
  35. Muscle tissue disease
  36. Muscular atrophy
  37. Muscular disease
  38. Muscular dystrophy
  39. Musculoskeletal system disease
  40. Myopathy
  41. Myopathy of extraocular muscle
  42. Nephronopthisis
  43. Nervous system disease
  44. Neuromuscular disease
  45. Neuropathy
  46. Ocular motility disease
  47. Oculocutaneous albinism
  48. Oculopharyngeal muscular dystrophy
  49. Optic atrophy
  50. Orbital disease
  51. Organ system cancer
  52. Pervasive developmental disease
  53. Physical disorder
  54. Prader-Willi syndrome
  55. Psychomotor disease
  56. Psychotic disease
  57. Schizoaffective disease
  58. Schizophrenia
  59. Sensory system disease
  60. Skin lipoma
  61. Specific developmental disease
  62. Spinal muscular atrophy
  63. Urinary system disease

Stage Associations

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