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Ask your administrator if you think this is wrong. ======= CD209 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: CD209 * **<color #00a2e8>Official Name</color>**: CD209 molecule * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=30835|30835]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q9NNX6|Q9NNX6]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=CD209&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20CD209|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/604672|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: This gene encodes a transmembrane receptor and is often referred to as DC-SIGN because of its expression on the surface of dendritic cells and macrophages. The encoded protein is involved in the innate immune system and recognizes numerous evolutionarily divergent pathogens ranging from parasites to viruses with a large impact on public health. The protein is organized into three distinct domains: an N-terminal transmembrane domain, a tandem-repeat neck domain and C-type lectin carbohydrate recognition domain. The extracellular region consisting of the C-type lectin and neck domains has a dual function as a pathogen recognition receptor and a cell adhesion receptor by binding carbohydrate ligands on the surface of microbes and endogenous cells. The neck region is important for homo-oligomerization which allows the receptor to bind multivalent ligands with high avidity. Variations in the number of 23 amino acid repeats in the neck domain of this protein are rare but have a significant impact on ligand binding ability. This gene is closely related in terms of both sequence and function to a neighboring gene (GeneID 10332; often referred to as L-SIGN). DC-SIGN and L-SIGN differ in their ligand-binding properties and distribution. Alternative splicing results in multiple variants.[provided by RefSeq, Feb 2009]. * **<color #00a2e8>UniProt Summary</color>**: N/A <button type='primary' size='sm' modal='Pfam_Domains'>Pfam Domains</button> <button type='primary' size='sm' modal='GO_terms'>GO Terms</button> <modal id='Pfam_Domains' size='lg' title='Pfam Domains'> |Lectin C| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |B cell adhesion| |peptide antigen transport| |virion attachment to host cell| |adhesion of symbiont to host cell| |virion binding| |adhesion of symbiont to host| |mannose binding| |viral genome replication| |modulation by virus of host morphology or physiology| |peptide antigen binding| |modification by symbiont of host morphology or physiology| |heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules| |leukocyte cell-cell adhesion| |intracellular transport of virus| |host cell| |transport of virus| |multi-organism transport| |cell-cell recognition| |multi-organism localization| |virus receptor activity| |viral entry into host cell| |positive regulation of T cell proliferation| |entry into host| |entry into host cell| |modification of morphology or physiology of other organism involved in symbiotic interaction| |stimulatory C-type lectin receptor signaling pathway| |innate immune response activating cell surface receptor signaling pathway| |positive regulation of lymphocyte proliferation| |positive regulation of mononuclear cell proliferation| |positive regulation of leukocyte proliferation| |modification of morphology or physiology of other organism| |interaction with host| |regulation of T cell proliferation| |carbohydrate binding| |antigen processing and presentation of peptide antigen| |viral life cycle| |positive regulation of T cell activation| |regulation of lymphocyte proliferation| |regulation of mononuclear cell proliferation| |antigen processing and presentation| |positive regulation of leukocyte cell-cell adhesion| |regulation of leukocyte proliferation| |innate immune response-activating signal transduction| |cell recognition| |positive regulation of cell-cell adhesion| |activation of innate immune response| |cell-cell adhesion via plasma-membrane adhesion molecules| |regulation of leukocyte cell-cell adhesion| |regulation of T cell activation| |positive regulation of innate immune response| |positive regulation of lymphocyte activation| |positive regulation of response to biotic stimulus| |external side of plasma membrane| |regulation of cell-cell adhesion| |positive regulation of cell adhesion| |positive regulation of leukocyte activation| |positive regulation of cell activation| |immune response-activating cell surface receptor signaling pathway| |regulation of innate immune response| |positive regulation of defense response| |immune response-regulating cell surface receptor signaling pathway| |cell-cell adhesion| |positive regulation of multi-organism process| |regulation of lymphocyte activation| |regulation of response to biotic stimulus| |endocytosis| |immune response-activating signal transduction| |immune response-regulating signaling pathway| |regulation of leukocyte activation| |positive regulation of response to external stimulus| |adaptive immune response| |cell surface| |activation of immune response| |regulation of cell activation| |import into cell| |regulation of cell adhesion| |viral process| |regulation of defense response| |innate immune response| |regulation of multi-organism process| |symbiotic process| |interspecies interaction between organisms| |positive regulation of immune response| |positive regulation of cell population proliferation| |cell adhesion| |biological adhesion| |defense response to other organism| |regulation of response to external stimulus| |positive regulation of immune system process| |regulation of immune response| |response to other organism| |response to external biotic stimulus| |response to biotic stimulus| |defense response| |regulation of response to stress| |peptide transport| |amide transport| |regulation of cell population proliferation| |regulation of immune system process| |intracellular signal transduction| |nitrogen compound transport| |immune response| |extracellular region| |vesicle-mediated transport| |membrane| </modal> \\ === CRISPR Data === <button type='default' size='small' modal='Compound_Hit'>Compound Hit</button> <button type='default' size='small' modal='Most_Correlated_Genes'>Most Correlated Genes in Chemogenomics</button> <button type='primary' size='small' modal='Essential_Avana'>Tissues where Essential in the Avana Dataset (DepMap 20Q1)</button> <modal id='Compound_Hit' size='lg' title='Compound Hit'> No hits were found. </modal> <modal id='Most_Correlated_Genes' size='lg' title='Most Correlated Genes in Chemogenomics'> No correlation found to any other genes in chemogenomics. </modal> <modal id='Essential_Avana' size='lg' title='Tissues where Essential in the Avana Dataset (DepMap 20Q1)'> Global Fraction of Cell Lines Where Essential: 0/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| </modal> == Essentiality in NALM6 == * **<color #00a2e8>Essentiality Rank</color>**: 15843 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 1.56 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='CD209 Expression in NALM6 Cells: 1.56'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2026/01/07 22:36by 127.0.0.1