| Gene Symbol | DLL3 |
| Entrez Gene ID | 10683 |
| Full Name | delta like canonical Notch ligand 3 |
| Synonyms | SCDO1 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| 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]. |
| Disorder MIM: | |
| Disorder Html: | Spondylocostal dysostosis 1, autosomal recessive, 277300 (3) |








































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