Gene Expression: PTER

Gene Data

  • Gene Symbol: PTER
  • Gene ID: 9317
  • Synonyms: HPHRP, RPR-1
  • Description: phosphotriesterase related
  • Database Refs: HGNC:9590, MIM:604446, Ensembl:ENSG00000165983, HPRD:16061, Vega:OTTHUMG00000017737
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 2 out of 7 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 95 diseases, scroll to view all:
  1. Acrocallosal syndrome
  2. Acute contagious conjunctivitis
  3. Amenorrhea
  4. Angelman syndrome
  5. Aniridia
  6. Atrial heart septal defect
  7. Atrioventricular septal defect
  8. Autism
  9. Autism spectrum disease
  10. Beckwith-Wiedemann syndrome
  11. Bone development disease
  12. Cancer
  13. Carcinoma
  14. Cell type cancer
  15. Chromosomal disease
  16. Cleft lip
  17. Cleft palate
  18. Coloboma
  19. Complex genetic disease
  20. Congenital heart defect
  21. Congenital nervous system abnormality
  22. Connective tissue neoplasm
  23. Cri-Du-Chat syndrome
  24. Cryptorchidism
  25. Developmental disease of mental health
  26. Dextrocardia
  27. Diaphragmatic eventration
  28. DiGeorge syndrome
  29. Disease
  30. Disease of anatomical entity
  31. Disease of cellular proliferation
  32. Disease of diaphragm
  33. Disease of mental health
  34. Down syndrome
  35. Dysostosis
  36. Ebstein anomaly
  37. Edwards syndrome
  38. Eye and adnexa disease
  39. Eye disease
  40. Female reproductive system disease
  41. Genetic disease
  42. Genitourinary cancer
  43. Globe disease
  44. Gonadal dysgenesis
  45. Heart septal defect
  46. Histiocytoma
  47. Holoprosencephaly
  48. Hydrocephalus
  49. Hydronephrosis
  50. Hypogonadism
  51. Hypospadias
  52. Imperforate anus
  53. Intellectual disability
  54. Kidney cancer
  55. Langer-Giedion syndrome
  56. Malignant fibroxanthoma
  57. Medical disorder
  58. Mesenchymal cell neoplasm
  59. Microcephaly
  60. Microphthalmia
  61. Mixed gonadal dysgenesis
  62. Monogenic disease
  63. Neoplasm of autonomic nervous system
  64. Nervous system cancer
  65. Nervous system disease
  66. Neuroblastoma
  67. Nodular tenosynovitis
  68. non-gestational choriocarcinoma
  69. Organ system cancer
  70. Orofacial cleft
  71. Patau syndrome
  72. Patent ductus arteriosus
  73. Peripheral nervous system neoplasm
  74. Pervasive developmental disease
  75. Physical disorder
  76. Pineal parenchymal tumor of intermediate
  77. Polydactyly
  78. Prader-Willi syndrome
  79. Primary immunodeficiency disease
  80. Pulmonary valve stenosis
  81. Reproductive system disease
  82. Sensory system disease
  83. Soft tissue cancer
  84. Specific developmental disease
  85. Syndactyly
  86. Synostosis
  87. Synovium neoplasm
  88. T cell deficiency
  89. Turner's syndrome
  90. Urinary tract cancer
  91. Urinary tract obstruction
  92. Ventricular septal defect
  93. Villonodular synovitis
  94. Wolf-Hirschhorn syndrome
  95. X-linked ichthyosis

Stage Associations

This gene is associated with the following stages: