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Basic information of NOS1 :

Official Symbol of Gene NOS1
Species Homo sapiens
Entrez Gene ID 4842
Official Full Name nitric oxide synthase 1
Also known as NOS; bNOS; nNOS; IHPS1; N-NOS; NC-NOS
Gene Type protein coding
dbXrefs Ensembl:ENSG00000089250 MIM:163731; AllianceGenome:HGNC:7872
Map Location 12q24.22
Variation Type allele
refSNP ID N/A

Sample information of multiple sclerosis:

Detected Sample peripheral blood
Sample Detail N/A
Detected Method PCR
Disease MS
Disease subtype RRMS,PPMS,SPMS
Population Caucasian Australian
Sample Size 104 MS / 104HCs

Literature information of multiple sclerosis :

Pubmed ID 14759629
Year 2007
Title Comparative expression of human endogenous retrovirus-W genes in multiple sclerosis

Results of multiple sclerosis :

Risk Type Disease risk
Main Result Negative
Result In this Australian population,13 alleles of this polymorphism were identified. This analysis indicates that the nNOS variant does not confer an altered effect on MS. Rank analysis also indicated that allelic distributions were not significantly different between test groups. Stratified analyses testing for a gender-specific relationship between MS and nNOS and comparisons of a specific clinical course group were also negative for association.
Mechanism/Pathway Nitric oxide (NO) production arising from nNOS has been involved in the pathophysiology of several disorders of the brain.NO has been shown to be toxic to oligodendrocytes and to induce axonal degeneration.Nitric oxide is also known to be a modulator of neuronal function affecting the release of neurotransmitters.