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NCBI Description of DLL3 |
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. |
Community Annotation of DLL3 Add / Edit DLL3: Annotations
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Figure notes
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Data details