Gene Expression: BGLAP

Gene Data

  • Gene Symbol: BGLAP
  • Gene ID: 632
  • Synonyms: BGP, OC, OCN
  • Description: bone gamma-carboxyglutamate (gla) protein
  • Database Refs: HGNC:1043, MIM:112260, HPRD:00205, Vega:OTTHUMG00000014819
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 4 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 155 diseases, scroll to view all:
  1. Acromegaly
  2. Adrenal cortex disease
  3. Adrenal gland disease
  4. Adrenal gland hyperfunction
  5. Amenorrhea
  6. Ankylosing spondylitis
  7. Ankylosis
  8. Arterial occlusive disease
  9. Arteriopathy
  10. Arteriosclerosis
  11. Arteriosclerotic cardiovascular disease
  12. Arthritis
  13. Arthropathy
  14. Asthma
  15. Atherosclerosis
  16. Autoimmune disease of endocrine system
  17. Autoimmune disease of urogenital tract
  18. Blood coagulation disease
  19. Bone cancer
  20. Bone development disease
  21. Bone disease
  22. Bone inflammation disease
  23. Bone marrow cancer
  24. Bone marrow disease
  25. Bone osteosarcoma
  26. Bone remodeling disease
  27. Bone resorption disease
  28. Bone tissue neoplasm
  29. Breast adenocarcinoma
  30. Breast cancer
  31. Breast carcinoma
  32. Bronchial disease
  33. Calcium metabolism disease
  34. Cancer
  35. Carbohydrate metabolism disease
  36. Cardiovascular system disease
  37. Cell type cancer
  38. Chronic kidney failure
  39. Cleidocranial dysplasia
  40. Connective tissue neoplasm
  41. Conventional central osteosarcoma
  42. Craniosynostosis
  43. Crohn's disease
  44. Cushing syndrome
  45. Dental fluorosis
  46. Diabetes mellitus
  47. Disease
  48. Disease of anatomical entity
  49. Disease of cellular proliferation
  50. Disease of metabolism
  51. Dysostosis
  52. End stage renal failure
  53. Endocrine pancreas disease
  54. Endocrine syndrome
  55. Endocrine system disease
  56. Familial hypophosphatemia
  57. Female reproductive system disease
  58. Fibrosarcomatous osteosarcoma
  59. Fibrous dysplasia
  60. Gastrointestinal system disease
  61. Genetic disease
  62. Genitourinary cancer
  63. Giant cell tumor
  64. Glucose metabolism disease
  65. Goiter
  66. Gonadal disease
  67. Graves' disease
  68. Hematologic cancer
  69. Hematopoietic system disease
  70. Hemiplegia
  71. Hemorrhagic disease
  72. Hepatobiliary disease
  73. Hereditary hypophosphatemic rickets
  74. Hypercalcemia
  75. Hyperostosis
  76. Hyperparathyroidism
  77. Hyperphosphatemia
  78. Hypersensitivity reaction disease
  79. Hypersensitivity reaction type II diseas
  80. Hyperthyroidism
  81. Hypogonadism
  82. Hypoparathyroidism
  83. Hypophosphatemia
  84. Hypothyroidism
  85. Immune system disease
  86. Impaired renal function disease
  87. Inborn errors metal metabolism
  88. Inborn errors of metabolism
  89. Inborn errors renal tubular transport
  90. Inflammatory bowel disease
  91. Intestinal disease
  92. Ischemic bone disease
  93. Juvenile rheumatoid arthritis
  94. Kidney disease
  95. Kidney failure
  96. Liver cirrhosis
  97. Liver disease
  98. Lower respiratory tract disease
  99. Lung disease
  100. Male reproductive organ cancer
  101. Mammary Paget's disease
  102. Medical disorder
  103. Mesenchymal cell neoplasm
  104. Mineral metabolism disease
  105. Monogenic disease
  106. Mouth disease
  107. Multiple myeloma
  108. Musculoskeletal system disease
  109. Myeloma
  110. Nervous system disease
  111. Nontoxic goiter
  112. Nutrition disease
  113. Nutritional deficiency disease
  114. Obstructive lung disease
  115. Organ system cancer
  116. Osteitis fibrosa
  117. Osteoarthritis
  118. Osteochondrodysplasia
  119. Osteogenesis imperfecta
  120. Osteomalacia
  121. Osteonecrosis
  122. Osteopetrosis
  123. Osteoporosis
  124. Osteosarcoma
  125. Osteosclerosis
  126. Paget's disease of bone
  127. Pancreas disease
  128. Parathyroid gland disease
  129. Periodontal disease
  130. Periodontitis
  131. Phosphorus metabolism disease
  132. Physical disorder
  133. Primary biliary cirrhosis
  134. Primary hyperparathyroidism
  135. Prostate cancer
  136. Renal osteodystrophy
  137. Reproductive organ cancer
  138. Reproductive system disease
  139. Respiratory system disease
  140. Rheumatoid arthritis
  141. Rickets
  142. Secondary hyperparathyroidism
  143. Soft tissue cancer
  144. SOST-related sclerosing bone dysplasia
  145. Synostosis
  146. Thoracic cancer
  147. Thyroid cancer
  148. Thyroid gland disease
  149. Thyroid neoplasm
  150. Thyrotoxicosis
  151. Tooth disease
  152. Ulcerative colitis
  153. Urinary system disease
  154. Vascular disease
  155. Vitamin K deficiency hemorrhagic disease

Stage Associations

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