NOS2 - nitric oxide synthase 2 Gene
Also Known as NOS; INOS; NOS2A; HEP-NOS
Species: Homo sapiens
About NOS2
This gene has 7 transcripts (splice variants), 166 orthologues, 5 paralogues and is associated with 1 phenotype. Biased expression in small intestine (RPKM 10.3), appendix (RPKM 7.9) and 5 other tissues.
Summary
Nitric oxide is a reactive free radical which acts as a biologic mediator in several processes, including neurotransmission and antimicrobial and antitumoral activities. This gene encodes a nitric oxide synthase which is expressed in liver and is inducible by a combination of lipopolysaccharide and certain cytokines. Three related pseudogenes are located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
NOS2 Products (2)
| mRNA | Protein | Name |
|---|---|---|
| NM_153292.1 | ||
| NM_000625.4 | NP_000616.3 | nitric oxide synthase, inducible |
NOS2 Protein Structure
NO_synthase: Nitric oxide synthase, oxygenase domain (132 - 502)
Flavodoxin_1: Flavodoxin (541 - 672)
FAD_binding_1: FAD binding domain (726 - 947)
NAD_binding_1: Oxidoreductase NAD-binding domain (979 - 1092)
- 0
- 200
- 400
- 600
- 800
- 1000
- 1153 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
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nitric oxide synthase, inducible |
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NOS2 Antibodies
| Cat. No. | Product Name | Application | Reactivity |
|---|---|---|---|
| HY-P80725 | iNOS Antibody | WB, IHC-P, IHC-F, ICC/IF | Human, Mouse, Rat |
| HY-P84272 | NOS2 Antibody (YA3969) | WB, IHC-P, FC, ELISA | Human, Mouse, Rat, Monkey |
| HY-P84272A | NOS2 Antibody (YA3969)(PBS only) | WB, IHC-P, FC, ELISA | Human, Mouse, Rat, Monkey |
| HY-P86080 | iNOS Antibody (YA5772) | WB, ICC/IF, IP, ELISA | Human, Mouse, Rat |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Malaria |
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| Periapical Granuloma |
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| Cardiovascular System Disease |
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| Acute Maxillary Sinusitis |
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| Breast Cancer |
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| Gastritis |
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| Peyronie Disease |
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| Chagas Disease |
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| Uremia |
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| Squamous Blepharitis |
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| Pre-Eclampsia |
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| Ischemia |
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| Pityriasis Lichenoides |
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| Hypertension, Essential |
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| Glomerulonephritis |
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| Adult Respiratory Distress Syndrome |
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| Spinal Cord Injury |
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| Multiple Sclerosis |
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| Constipation |
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| Primary Ciliary Dyskinesia |
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| Colitis |
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| Congenital Hypothyroidism |
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| Hepatopulmonary Syndrome |
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| Diabetes Mellitus |
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| Meningioma, Familial |
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| Atherosclerosis Susceptibility |
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| Trichothiodystrophy 7, Nonphotosensitive |
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| Orthostatic Intolerance |
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| Microvascular Complications Of Diabetes 5 |
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| Encephalitis |
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| Smith-Magenis Syndrome |
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| Microcephaly |
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| Colorectal Cancer |
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| Retinal Vasculitis |
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| Hyperglycemia |
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| Impotence |
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| Chlamydia |
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| Amyotrophic Lateral Sclerosis 3 |
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| Vascular Disease |
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| Inflammatory Bowel Disease |
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| Peripheral T-Cell Lymphoma |
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| Type 1 Diabetes Mellitus |
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| Pulmonary Hypertension |
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| Cerebral Palsy |
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| Lipoprotein Quantitative Trait Locus |
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| Myocarditis |
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| Baritosis |
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| Pulmonary Edema |
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| Collagenous Colitis |
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| Lung Cancer |
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| Brain Edema |
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| Supraglottis Squamous Cell Carcinoma |
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| Toxic Shock Syndrome |
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| Nervous System Disease |
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| Alzheimer Disease, Familial, 1 |
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| Achalasia |
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| Plasmodium Falciparum Malaria |
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| Heart Disease |
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| Ureteral Obstruction |
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| Priapism |
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| Marfan Syndrome |
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| Arthus Reaction |
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| Proteasome-Associated Autoinflammatory Syndrome 1 |
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| Mucositis |
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| Pulpitis |
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| Cystic Fibrosis |
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| Visceral Leishmaniasis |
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| Mycetoma |
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| Myocardial Infarction |
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| Asbestosis |
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| Acquired Immunodeficiency Syndrome |
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| Filariasis |
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| Chlorhexidine Allergy |
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| Asthma |
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| Hepatocellular Carcinoma |
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| Wilson Disease |
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| Leishmaniasis |
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| Glioblastoma |
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Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Felis catus | NOS2 | VGNC | VGNC:68514 |
| Canis familiaris | NOS2 | VGNC | VGNC:43895 |
| Macaca mulatta | NOS2 | VGNC | VGNC:75369 |
| Bos taurus | NOS2 | VGNC | VGNC:32173 |
| Rattus norvegicus | NOS2 | RGD | RGD:3185 |
| Mus musculus | NOS2 | MGD | MGI:97361 |
| Others | NOS2 | NCBI |