Gene
DLL4
delta like canonical Notch ligand 4
- HGNC 2910↗(opens in a new tab)
- Ensembl gene ENSG00000128917↗(opens in a new tab)
- NCBI Gene 54567↗(opens in a new tab)
Summary
- Cytogenetic location
- 15q15.1
- Coordinates
- Chromosome 15: 40,929,340–40,939,073 (GRCh38)
- Exons
- 11 exons across 9.7 kb
- Protein
- 685 amino acids
- MANE Select transcript
- ENST00000249749.7NM_019074.4
- 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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No Genome Test report reads DLL4 yet. The test sequences your whole genome, so your data includes it all the same.
How DLL4 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 3.4 kb of the gene's 9.7 kb; 2,058 of those bases code for the protein.
How a genome test reads DLL4
21
positions in DLL4 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 9.7 kb of DLL4, introns included, not only the 3.4 kb of exons.
Traits linked to DLL4
The Human Phenotype Ontology lists these as features of the rare conditions DLL4 can cause. Each trait's page lists the other genes linked to it.
Abnormality of limbs
- Abnormality of the lower limb
- Abnormality of the upper limb
- Absent hand
- Absent toe
- Abnormal shape of long bones of hand
- Finger syndactyly
- Short fingers or toes
- Short outermost finger bone
Show 5 more traits
Abnormality of the integument
- Absence of part of skin at birth
- Absent/small skin
- Aplasia cutis congenita over the scalp vertex
- Congenital localized absence of skin
- Sparse hair
- Focal absence of scalp tissue
- Open skin sore
- Absent fingernail
Show 4 more traits
Abnormality of the nervous system
- Spinal dysraphism
- Too much cerebrospinal fluid in the brain
- Cavity within brain
- EEG abnormality
- Epilepsy
- Intellectual disability
- Periventricular leukomalacia
- Tactile hypersensitivity
Show 1 more trait
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.). DLL4 gene: delta like canonical Notch ligand 4. Retrieved 17 October 2026, from https://dantelabs.com/genes/dll4
Dante Labs. DLL4 gene: delta like canonical Notch ligand 4 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/dll4
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