======= SPG11 ======= == Gene Information == * **Official Symbol**: SPG11 * **Official Name**: SPG11 vesicle trafficking associated, spatacsin * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=80208|80208]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q96JI7|Q96JI7]] * **Interactions**: [[https://thebiogrid.org/search.php?search=SPG11&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20SPG11|Open PubMed]] * **OMIM**: [[https://omim.org/entry/610844|Open OMIM]] == Function Summary == * **Entrez Summary**: The protein encoded by this gene is a potential transmembrane protein that is phosphorylated upon DNA damage. Defects in this gene are a cause of spastic paraplegia type 11 (SPG11). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]. * **UniProt Summary**: N/A No Pfam Domain information is available for this gene. |phagosome-lysosome fusion involved in apoptotic cell clearance| |phagosome maturation involved in apoptotic cell clearance| |phagolysosome assembly involved in apoptotic cell clearance| |phagosome-lysosome fusion| |phagolysosome assembly| |walking behavior| |synaptic vesicle transport| |axon extension| |apoptotic cell clearance| |synaptic vesicle localization| |phagosome maturation| |lytic vacuole organization| |lysosome organization| |neuron projection extension| |axo-dendritic transport| |vesicle fusion| |organelle membrane fusion| |developmental cell growth| |cell growth| |organelle fusion| |developmental growth involved in morphogenesis| |vacuole organization| |membrane fusion| |transport along microtubule| |establishment of vesicle localization| |cytoskeleton-dependent intracellular transport| |microtubule-based transport| |vesicle localization| |locomotory behavior| |cytoplasmic vesicle| |synapse| |microtubule-based movement| |axon| |lysosomal membrane| |vesicle organization| |phagocytosis| |establishment of organelle localization| |axonogenesis| |developmental growth| |growth| |axon development| |chemical synaptic transmission| |dendrite| |anterograde trans-synaptic signaling| |cell morphogenesis involved in neuron differentiation| |trans-synaptic signaling| |synaptic signaling| |neuron projection morphogenesis| |plasma membrane bounded cell projection morphogenesis| |cell projection morphogenesis| |cell part morphogenesis| |cell morphogenesis involved in differentiation| |behavior| |organelle localization| |neuron projection development| |microtubule-based process| |cell morphogenesis| |organelle assembly| |neuron development| |cellular component morphogenesis| |membrane organization| |nucleolus| |neuron differentiation| |cell-cell signaling| |plasma membrane bounded cell projection organization| |cell projection organization| |intracellular transport| |generation of neurons| |movement of cell or subcellular component| |neurogenesis| |cell development| |establishment of localization in cell| |vesicle-mediated transport| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp222|Betulinic acid 10 to 15μM on day4 R05 exp222]]|-2.31| |[[:results:exp246|UM0011500 10μM R05 exp246]]|-2.13| |[[:results:exp180|Dynasore 10μM R04 exp180]]|1.71| 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**: 5044 * **Expression level (log2 read counts)**: 6.92 {{:chemogenomics:nalm6 dist.png?nolink |}}