NOS1 (nitric oxide synthase 1)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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4842 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Nitric oxide synthase 1 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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NOS1 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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IHPS1, N-NOS, NC-NOS, NOS, bNOS, nNOS |
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Chromosome
Chromosome number
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12 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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12q24.22 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene belongs to the family of nitric oxide synthases, which synthesize nitric oxide from L-arginine. Nitric oxide is a reactive free radical, which acts as a biologic mediator in several processes, including neurotransmission, |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||||||||||||||||||||||
| UniProt ID | P29475 | ||||||||||||||||||||||||||||||
| Protein name | Nitric oxide synthase 1 (EC 1.14.13.39) (Constitutive NOS) (NC-NOS) (NOS type I) (Neuronal NOS) (N-NOS) (nNOS) (Nitric oxide synthase, brain) (bNOS) (Peptidyl-cysteine S-nitrosylase NOS1) | ||||||||||||||||||||||||||||||
| Protein function | Produces nitric oxide (NO) which is a messenger molecule with diverse functions throughout the body. In the brain and peripheral nervous system, NO displays many properties of a neurotransmitter. Probably has nitrosylase activity and mediates cy | ||||||||||||||||||||||||||||||
| PDB | 4D1N , 4UCH , 4UH5 , 4UH6 , 4V3U , 5ADF , 5ADG , 5ADI , 5FVU , 5FVV , 5FVW , 5FVX , 5UO1 , 5UO2 , 5UO3 , 5UO4 , 5UO5 , 5UO6 , 5UO7 , 5VUV , 5VUW , 5VUX , 5VUY , 5VUZ , 5VV0 , 5VV1 , 5VV2 , 5VV3 , 5VV4 , 5VV5 , 6AUY , 6AUZ , 6AV0 , 6AV1 , 6AV2 , 6AV3 , 6AV4 , 6AV5 , 6CIC , 6CID , 6NG1 , 6NG2 , 6NG4 , 6NG5 , 6NG6 , 6NG7 , 6NG8 , 6NGA , 6NGB , 6NGC , 6NGD | ||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Isoform 1 is ubiquitously expressed: detected in skeletal muscle and brain, also in testis, lung and kidney, and at low levels in heart, adrenal gland and retina. Not detected in the platelets. Isoform 3 is expressed only in testis. Is | ||||||||||||||||||||||||||||||
| Sequence | |||||||||||||||||||||||||||||||
| Sequence length | 1434 | ||||||||||||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||||||||||||
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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