Gene
DCC
DCC netrin 1 receptor
- HGNC 2701↗(opens in a new tab)
- Ensembl gene ENSG00000187323↗(opens in a new tab)
- NCBI Gene 1630↗(opens in a new tab)
Summary
- Cytogenetic location
- 18q21.2
- Coordinates
- Chromosome 18: 52,340,197–53,535,899 (GRCh38)
- Exons
- 29 exons across 1,195.7 kb
- Protein
- 1,447 amino acids
- Also known as
- IGDCC1, NTN1R1
- MANE Select transcript
- ENST00000442544.7NM_005215.4
- 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 DCC yet. The test sequences your whole genome, so your data includes it all the same.
How DCC is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
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 10.2 kb of the gene's 1,195.7 kb; 4,344 of those bases code for the protein.
How a genome test reads DCC
21
positions in DCC 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 1,195.7 kb of DCC, introns included, not only the 10.2 kb of exons.
Traits linked to DCC
The Human Phenotype Ontology lists these as features of the rare conditions DCC can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Abnormality of the anterior commissure
- Absent hippocampal commissure
- Agenesis of corpus callosum
- Global developmental delay
- Hypoplasia of the pons
- Midline brainstem cleft
- Abnormal corticospinal tract morphology
- Abnormality of movement
Show 22 more traits
- Clumsiness
- Cognitive impairment
- Delayed speech and language development
- Fusion of the left and right thalami
- Hand mirror movements
- Intellectual disability
- Interhemispheric cyst
- Poor fine motor coordination
- Abnormal gait
- Ataxia
- Difficulty articulating speech
- Dysgenesis of the hippocampus
- Epilepsy
- Increased reflexes
- Leg paralysis
- Specific learning disability
- Too much cerebrospinal fluid in the brain
- Tremor
- Unsteady walk
- Weakness of one side of body
- Cerebral palsy
- Intellectual disability, mild
Abnormality of the musculoskeletal system
- Hunched back
- Scoliosis
- Delayed bone maturation
- Low muscle tone
- Low solidness and mass of the bones
- Muscle tissue disease
- Tired easily
- Abnormal skeletal development
Show 3 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.). DCC gene: DCC netrin 1 receptor. Retrieved 17 October 2026, from https://dantelabs.com/genes/dcc
Dante Labs. DCC gene: DCC netrin 1 receptor [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/dcc
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