Gene entry
DCX
doublecortin
- Chromosome
- X
- Cytoband
- Xq23
- Variants (rsID)
- 17
DCX is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq23). Its official name is “doublecortin”. The reference table lists 17 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs587783569Likely pathogenicsingle nucleotide variantHeterotopia
- rs104894780Pathogenicsingle nucleotide variantSubcortical laminar heterotopia, X-linked|Lissencephaly type 1 due to doublecortin gene mutation|Heterotopia
- rs104894782Pathogenicsingle nucleotide variantSubcortical laminar heterotopia, X-linked|Lissencephaly type 1 due to doublecortin gene mutation|Neurodevelopmental disorder
- rs104894784Pathogenicsingle nucleotide variantSubcortical laminar heterotopia, X-linked
- rs104894785Pathogenicsingle nucleotide variantSubcortical laminar heterotopia, X-linked
- rs122457137Pathogenicsingle nucleotide variantLissencephaly type 1 due to doublecortin gene mutation|Subcortical laminar heterotopia, X-linked
- rs201870761Pathogenicsingle nucleotide variantHeterotopia
- rs267606317Pathogenicsingle nucleotide variantHeterotopia
- rs56030372Pathogenicsingle nucleotide variantLissencephaly type 1 due to doublecortin gene mutation|Subcortical laminar heterotopia, X-linked|Heterotopia|Abnormal cerebral morphology
- rs587783568Pathogenicsingle nucleotide variantHeterotopia|Lissencephaly type 1 due to doublecortin gene mutation
- rs61729440Pathogenicsingle nucleotide variantHeterotopia
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.