DLL3


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].

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GO terms in DLL3


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Term Type
Evidence Type
GO Term ID
GO Des.
MF NAS GO:0005112 Notch binding
MF IEA GO:0005509 calcium ion binding
BP IMP GO:0001501 skeletal system development
BP IEA GO:0001756 somitogenesis
BP IEA GO:0007219 Notch signaling pathway
BP IEA GO:0007386 compartment pattern specification
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Gene expression in normal tissue: DLL3

Gene-model tissue-cancer distribution: Bubble Plot

undefinetissue: undefine cancer: undefined model num: 0undefinedtissue: undefined cancer: PANCAN model num: 2

Gene-drug pathway distribution

Pathways in DLL3


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Database
Pathway ID
Pathway Des.
wikipathways WP2064 Neural Crest Differentiation
wikipathways WP268 Notch Signaling Pathway
wikipathways WP3413 NOTCH1 regulation of human endothelial cell calcification
wikipathways WP3845 Canonical and Non-canonical Notch signaling
wikipathways WP4239 EMT transition in Colorectal Cancer
wikipathways WP4242 Notch Signaling Pathway
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD309 17AAG 1
iGMDRD491 TAE-684 1
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in DLL3

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

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