======= MBL2 ======= == Gene Information == * **Official Symbol**: MBL2 * **Official Name**: mannose binding lectin 2 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=4153|4153]] * **UniProt**: [[https://www.uniprot.org/uniprot/P11226|P11226]] * **Interactions**: [[https://thebiogrid.org/search.php?search=MBL2&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20MBL2|Open PubMed]] * **OMIM**: [[https://omim.org/entry/154545|Open OMIM]] == Function Summary == * **Entrez Summary**: This gene encodes the soluble mannose-binding lectin or mannose-binding protein found in serum. The protein encoded belongs to the collectin family and is an important element in the innate immune system. The protein recognizes mannose and N-acetylglucosamine on many microorganisms, and is capable of activating the classical complement pathway. Deficiencies of this gene have been associated with susceptibility to autoimmune and infectious diseases. [provided by RefSeq, Jul 2008]. * **UniProt Summary**: N/A |Collagen| |Lectin C| |opsonization| |killing by host of symbiont cells| |disruption by host of symbiont cells| |complement activation, lectin pathway| |killing of cells in other organism involved in symbiotic interaction| |disruption of cells of other organism involved in symbiotic interaction| |growth plate cartilage chondrocyte morphogenesis| |chondrocyte morphogenesis| |chondrocyte morphogenesis involved in endochondral bone morphogenesis| |growth plate cartilage morphogenesis| |mannose binding| |growth plate cartilage chondrocyte differentiation| |chondrocyte development involved in endochondral bone morphogenesis| |cartilage morphogenesis| |chondrocyte differentiation involved in endochondral bone morphogenesis| |growth plate cartilage development| |acute-phase response| |endochondral bone growth| |chondrocyte development| |bone growth| |cartilage development involved in endochondral bone morphogenesis| |disruption of cells of other organism| |killing of cells of other organism| |collagen trimer| |calcium-dependent protein binding| |positive regulation of phagocytosis| |acute inflammatory response| |modification by host of symbiont morphology or physiology| |endochondral bone morphogenesis| |interaction with symbiont| |chondrocyte differentiation| |cell killing| |defense response to Gram-positive bacterium| |regulation of phagocytosis| |organ growth| |negative regulation of viral process| |modification of morphology or physiology of other organism involved in symbiotic interaction| |bone morphogenesis| |modification of morphology or physiology of other organism| |complement activation, classical pathway| |humoral immune response mediated by circulating immunoglobulin| |cartilage development| |complement activation| |bone development| |regulation of viral process| |immunoglobulin mediated immune response| |B cell mediated immunity| |negative regulation of multi-organism process| |regulation of symbiosis, encompassing mutualism through parasitism| |connective tissue development| |extracellular matrix| |skeletal system morphogenesis| |lymphocyte mediated immunity| |adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains| |phagocytosis| |defense response to bacterium| |signaling receptor binding| |humoral immune response| |collagen-containing extracellular matrix| |response to oxidative stress| |developmental growth| |growth| |skeletal system development| |inflammatory response| |regulation of vesicle-mediated transport| |cell morphogenesis involved in differentiation| |tissue morphogenesis| |adaptive immune response| |cell surface| |activation of immune response| |response to bacterium| |calcium ion binding| |cell morphogenesis| |innate immune response| |leukocyte mediated immunity| |regulation of multi-organism process| |symbiotic process| |interspecies interaction between organisms| |cellular component morphogenesis| |positive regulation of immune response| |defense response to other organism| |animal organ morphogenesis| |positive regulation of transport| |immune effector process| |regulation of immune response| |positive regulation of immune system process| |response to other organism| |response to external biotic stimulus| |response to biotic stimulus| |defense response| |extracellular space| |cell development| |regulation of immune system process| |tissue development| |regulation of transport| |immune response| |extracellular region| |vesicle-mediated transport| \\ === CRISPR Data === No hits were found. No correlation found to any other genes in chemogenomics. 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| == Essentiality in NALM6 == * **Essentiality Rank**: 10759 * **Expression level (log2 read counts)**: -4.27 {{:chemogenomics:nalm6 dist.png?nolink |}}