======= DLL3 ======= == Gene Information == * **Official Symbol**: DLL3 * **Official Name**: delta like canonical Notch ligand 3 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=10683|10683]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q9NYJ7|Q9NYJ7]] * **Interactions**: [[https://thebiogrid.org/search.php?search=DLL3&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20DLL3|Open PubMed]] * **OMIM**: [[https://omim.org/entry/602768|Open OMIM]] == Function Summary == * **Entrez Summary**: This gene encodes a member of the delta protein ligand family. This family functions as Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. Mutations in this gene cause autosomal recessive spondylocostal dysostosis 1. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]. * **UniProt Summary**: Inhibits primary neurogenesis. May be required to divert neurons along a specific differentiation pathway. Plays a role in the formation of somite boundaries during segmentation of the paraxial mesoderm (By similarity). {ECO:0000250}. |EGF| |MNNL| |compartment pattern specification| |paraxial mesoderm development| |Notch binding| |somitogenesis| |somite development| |segmentation| |mesoderm development| |Notch signaling pathway| |anterior/posterior pattern specification| |mesenchyme development| |negative regulation of neurogenesis| |negative regulation of nervous system development| |regionalization| |negative regulation of cell development| |pattern specification process| |skeletal system development| |chordate embryonic development| |embryo development ending in birth or egg hatching| |negative regulation of cell differentiation| |calcium ion binding| |regulation of neurogenesis| |anatomical structure formation involved in morphogenesis| |regulation of nervous system development| |regulation of cell development| |negative regulation of developmental process| |embryo development| |epithelium development| |negative regulation of multicellular organismal process| |generation of neurons| |neurogenesis| |tissue development| |regulation of cell differentiation| \\ === 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**: 5171 * **Expression level (log2 read counts)**: 2.39 {{:chemogenomics:nalm6 dist.png?nolink |}}