DSC1
Chr 18desmocollin 1
Also known as: CDHF1, DG2/DG3
Desmocollin-1 is a calcium-dependent adhesive glycoprotein that forms desmosome cell-cell junctions in epithelial cells, maintaining epidermal barrier function and normal hair follicle morphology. Mutations cause autosomal recessive striate palmoplantar keratoderma with woolly hair and cardiomyopathy, affecting the skin and cardiac systems. This gene is extremely tolerant to loss-of-function variants (pLI near zero), suggesting the pathogenic variants likely act through other mechanisms.
Population Genetics & Constraint
gnomAD v4 — loss-of-function & missense intolerance
Typical tolerance to LoF variation
Tolerant to missense variation
This gene has evidence for multiple mechanisms of pathogenicity (dominant-negative and gain-of-function). Both the Badonyi & Marsh prediction and the broader genomic evidence point to dominant-negative as the predominant mechanism. Different variants in this gene may act through different mechanisms — interpret in context of the specific variant.
Note: In-silico variant effect predictors (SIFT, PolyPhen, REVEL, CADD) may underestimate pathogenicity of missense variants in genes with GOF or DN mechanisms. Consider functional evidence and clinical context.
Predictions from Badonyi M, Marsh JA. PLoS ONE. 2024;19(8):e0307312.
ClinVar Variant Classifications
0 submitted variants in ClinVar
Protein Context — Lollipop Plot
DSC1 · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
3D Protein StructureAlphaFold
External Resources
Links to major genomics databases and tools
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →External Resources
Links to major genomics databases and tools