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}.
Pfam DomainsGO Terms
Pfam Domains
EGF
MNNL
GO Terms
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
Compound HitMost Correlated Genes in ChemogenomicsTissues where Essential in the Avana Dataset (DepMap 20Q1)
Compound Hit
No hits were found.
Most Correlated Genes in Chemogenomics
No correlation found to any other genes in chemogenomics.
Tissues where Essential in the Avana Dataset (DepMap 20Q1)
Global Fraction of Cell Lines Where Essential: 0/739