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Gene Symbol |
HMOX1 |
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Aliases |
HMOX1D, HO-1, HSP32, bK286B10 |
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Entrez Gene ID |
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Gene Name |
Heme oxygenase 1 |
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Chromosomal Location |
22q12.3 |
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HGNC ID |
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Summary |
Heme oxygenase, an essential enzyme in heme catabolism, cleaves heme to form biliverdin, which is subsequently converted to bilirubin by biliverdin reductase, and carbon monoxide, a putative neurotransmitter. Heme oxygenase activity is induced by its substrate heme and by various nonheme substances. Heme oxygenase occurs as 2 isozymes, an inducible heme oxygenase-1 and a constitutive heme oxygenase-2. HMOX1 and HMOX2 belong to the heme oxygenase family. [provided by RefSeq, Jul 2008]
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RefSeq DNA |
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RefSeq mRNA |
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e!Ensembl
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Protein Information |
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Protein Name |
Heme oxygenase 1, heat shock protein, 32-kD, heme oxygenase (decycling) 1 |
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Function |
Heme oxygenase cleaves the heme ring at the alpha methene bridge to form biliverdin. Biliverdin is subsequently converted to bilirubin by biliverdin reductase. Under physiological conditions, the activity of heme oxygenase is highest in the spleen, where senescent erythrocytes are sequestrated and destroyed. Exhibits cytoprotective effects since excess of free heme sensitizes cells to undergo apoptosis |
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UniProt |
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PDB |
1N3U, 1N45, 1NI6, 1OYK, 1OYL, 1OZE, 1OZL, 1OZR, 1OZW, 1S13, 1S8C, 1T5P, 1TWN, 1TWR, 1XJZ, 1XK0, 1XK1, 1XK2, 1XK3, 3CZY, 3HOK, 3K4F, 3TGM, 4WD4, 5BTQ, 6EHA |
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Pfam |
Pfam Accession |
Pfam ID |
PF01126 |
Heme_oxygenase |
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Interactions |
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STRING |
MINT |
IntAct |
ENSP00000252486 |
P02649 |
P02649 |
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View interactions
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Associated Diseases
Disease group | Disease Name | References |
Blood Disorders |
Anemia |
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Blood Coagulation Disorders |
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Cardiovascular Diseases |
Hypertensive disease |
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Heart Failure |
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Diabetic Cardiomyopathies |
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Myocardial Ischemia |
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Arteriosclerosis |
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Myocardial Failure |
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Digestive System Diseases |
Liver Diseases |
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Hepatorenal Syndrome |
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Gastroparesis |
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Colitis |
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Pancreatic Diseases |
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Hepatitis |
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Endocrine System Diseases |
Diabetes Mellitus |
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PCOS |
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Eye Diseases |
Retinal Diseases |
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Neoplasms |
Gastric Cancer |
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Stomach Cancer |
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Carotid Atherosclerosis |
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Prostate cancer |
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Lung Cancer |
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Breast Cancer |
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Liver Cancer |
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Mastocytosis |
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Nervous System Diseases |
Degenerative Diseases Central Nervous System |
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Status Epilepticus |
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Petit mal status |
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Carotid Artery Diseases |
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Moyamoya disease |
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Spinocerebellar ataxia |
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Parkinson Disease |
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Adrenoleukodystrophy |
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Adrenomyeloneuropathy |
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Nutritional and Metabolic Diseases |
Obesity |
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Hyperinsulinism |
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Iron Metabolism Disorders |
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Gluocose Intolerance |
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Psychiatric/Brain disorders |
Alzheimer Disease |
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Learning Disorders |
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Senile Dementia |
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Schizophrenia |
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Obstructive Sleep Apnea |
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Renal Disorder |
Kidney Failure |
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Kidney Insufficiency |
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Reproductive disorders |
Preeclampsia |
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Respiratory Tract Diseases |
Pneumonia |
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Asthma |
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Pulmonary Emphysema |
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Pulmonary Fibrosis |
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Emphysema |
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Chronic Lung Injury |
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Skin and Connective Tissue Diseases |
Dermatitis |
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References |
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PubMed ID |
Associated gene/s |
Associated condition |
Genetic Mutation |
Diagnostic Criteria |
Association with PCOS |
Ethnicity |
Conclusion |
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Insulin resistance and glucose tolerance |
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Rotterdam criteria |
Related
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Our results suggest that the HO-1-adiponectin axis may be associated with the regulation of insulin resistance and glucose intolerance in women with PCOS. |
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