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Gene : DLL3 Homo sapiens

Name  ? delta like canonical Notch ligand 3 Cytological Location  19q13.2
Brief Description  delta like canonical Notch ligand 3
Description  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]
  • synonyms:
  • OTTHUMG00000183067,
  • HGNC:2909,
  • SCDO1,
  • DLL3,
  • SCDO1,
  • delta-like 3 (Drosophila),
  • delta (Drosophila)-like 3,
  • AF241373,
  • uc002olw.3,
  • NM_016941
  • identifiers:
  • 10683,
  • ENSG00000090932,
  • DLL3

Genome feature

Region: gene ? Length: 9523  
Location: 19:39498947-39508469 Cyto location: 19q13.2


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

167 SN Ps

4 Cross References

16 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results