Gene
DLL1
delta like canonical Notch ligand 1
- HGNC 2908↗(opens in a new tab)
- Ensembl gene ENSG00000198719↗(opens in a new tab)
- NCBI Gene 28514↗(opens in a new tab)
Summary
- Cytogenetic location
- 6q27
- Coordinates
- Chromosome 6: 170,282,206–170,291,078 (GRCh38)
- Exons
- 11 exons across 8.9 kb
- Protein
- 723 amino acids
- MANE Select transcript
- ENST00000366756.4NM_005618.4
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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How DLL1 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 3.8 kb of the gene's 8.9 kb; 2,172 of those bases code for the protein.
How a genome test reads DLL1
35
positions in DLL1 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 8.9 kb of DLL1, introns included, not only the 3.8 kb of exons.
Traits linked to DLL1
The Human Phenotype Ontology lists these as features of the rare conditions DLL1 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Global developmental delay
- Abnormal central motor function
- Abnormal corpus callosum morphology
- Abnormal morphology of the olfactory bulb
- Abnormal shape of brain
- Abnormal shape of brainstem
- Abnormal shape of midbrain
- Abnormality of the autonomic nervous system
Show 35 more traits
- Absent speech development
- Anxiety
- Aplasia of the falx cerebri
- Attention deficit
- Autism spectrum disorder
- Behavioral abnormality
- Communication delay
- Depression
- Epilepsy
- Impulsivity
- Inability to walk
- Intellectual disability
- Irritability
- Lack of feeling, emotion, interest
- Lethargy
- Limb dystonia
- Neural tube defect
- Oromotor apraxia
- Poor speech
- Short attention span
- Sleep-wake cycle disturbance
- Specific learning disability
- Ventriculomegaly
- Abnormal septum pellucidum morphology
- Abnormality of neuronal migration
- Agenesis of corpus callosum
- Ataxia
- Cortical dysplasia
- Enlarged brain
- Holoprosencephaly
- Hypoplasia of the pons
- Perisylvian polymicrogyria
- Repetitive movements
- Rhombencephalosynapsis
- Too much cerebrospinal fluid in the brain
Abnormality of the digestive system
- Feeding difficulties
- Poor suck
- Acid reflux
- Constipation
- Poor swallowing
- Vomiting
- Abnormal shape of the digestive system
- Absence or narrowing of first part of small bowel
Show 2 more traits
Abnormality of the endocrine system
- Abnormal hypothalamus physiology
- Abnormality of the endocrine system
- Anterior hypopituitarism
- Central diabetes insipidus
- Diabetes insipidus
- Early onset of puberty
- Central hypothyroidism
- Decreased response to growth hormone stimulation test
Show 2 more traits
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). DLL1 gene: delta like canonical Notch ligand 1. Retrieved 17 October 2026, from https://dantelabs.com/genes/dll1
Dante Labs. DLL1 gene: delta like canonical Notch ligand 1 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/dll1
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