Gene
DCX
doublecortin
- HGNC 2714↗(opens in a new tab)
- Ensembl gene ENSG00000077279↗(opens in a new tab)
- NCBI Gene 1641↗(opens in a new tab)
Summary
- Cytogenetic location
- Xq23
- Coordinates
- Chromosome X: 111,293,779–111,412,192 (GRCh38)
- Exons
- 7 exons across 118.4 kb
- Protein
- 366 amino acids
- Also known as
- SCLH, DC, LISX, DBCN, XLIS
- MANE Select transcript
- ENST00000636035.2NM_001195553.2
- 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 DCX yet. The test sequences your whole genome, so your data includes it all the same.
How DCX 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 9.1 kb of the gene's 118.4 kb; 1,101 of those bases code for the protein.
How a genome test reads DCX
38
positions in DCX 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 118.4 kb of DCX, introns included, not only the 9.1 kb of exons.
Traits linked to DCX
The Human Phenotype Ontology lists these as features of the rare conditions DCX can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Behavioral abnormality
- Cognitive impairment
- Epilepsy
- Language impairment
- Agyria
- Akinetic mutism
- Cerebral palsy
- Fewer and broader ridges in brain
Show 21 more traits
- Generalized-onset seizure
- Infantile spasms
- Poor gross motor coordination
- Seizure affecting one half of brain
- Abnormal caudate nucleus morphology
- Agitation
- Autism spectrum disorder
- Cerebral white matter atrophy
- Delayed myelination
- Epileptic encephalopathy
- Hypsarrhythmia
- Irritability
- Lateral ventricle dilatation
- Underdevelopment of part of brain called corpus callosum
- Agenesis of corpus callosum
- Ataxia
- Difficulty articulating speech
- Fewer or absent grooves in brain
- Gray matter heterotopia
- Intellectual disability
- Motor delay
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.). DCX gene: doublecortin. Retrieved 16 October 2026, from https://dantelabs.com/genes/dcx
Dante Labs. DCX gene: doublecortin [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/dcx
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