In silico screening and identification of deleterious missense SNPs along with their effects on CD-209 gene: An insight to CD-209 related-diseases.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 33635927.
- Also identified by DOI 10.1371/journal.pone.0247249 and PMC identifier 7909662.
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Abstract
DC-SIGN receptor articulated by macrophages and dendritic cells is encoded by CD209 gene and plays a role to activate and proliferate the T-lymphocytes in response of virus attack. The dysfunctional activity of DC-SIGN receptor because of missense SNPs can lead to cause dengue haemorrhage fever, HIV-1 infection etc. Out of 11 transcripts of CD209, all missense SNPs of canonical transcript were retrieved from Ensembl database and evaluated by their deleteriousness by using Polyphen-2, PMut, SIFT, MutPred, PROVEAN and PhD-SNP together with stimulation of its complete 3D structure. 10 nsSNPs were chosen depending on both the significance value of nsSNP and their prediction among SNPs evaluating servers which are based on different algorithms. Moreover, the position and native role of 10 nsSNPs in wild 3D model has been described which assist to acknowledge their importance. This study urges the researcher's community to experimentally validate these SNPs and their association in causing the diseases like dengue fever, Tuberculosis etc.
Medical subject headings
- Cell Adhesion Molecules
- Cell Adhesion Molecules/chemistry
- Cell Adhesion Molecules/genetics
- Computational Biology
- Computational Biology/methods
- Computer Simulation
- Genetic Predisposition to Disease
- Humans
- Hydrogen Bonding
- Lectins, C-Type
- Lectins, C-Type/chemistry
- Lectins, C-Type/genetics
- Models, Molecular
- Mutation, Missense
- Polymorphism, Single Nucleotide
- Protein Conformation
- Protein Stability
- Receptors, Cell Surface
- Receptors, Cell Surface/chemistry
- Receptors, Cell Surface/genetics
- Software
- DC-Specific ICAM-3 Grabbing Nonintegrin