Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

CCDC39

coiled-coil domain 39 molecular ruler complex subunit

Chromosome
3
Cytoband
3q26.33
Variants (rsID)
23

CCDC39 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q26.33). Its official name is “coiled-coil domain 39 molecular ruler complex subunit”. The reference table lists 23 variants (rsID) for this gene.

Clinically classified variants

18 reference-table entries with clinical significance.

  • rs115545935Benignsingle nucleotide variantPrimary ciliary dyskinesia 14|Primary ciliary dyskinesia
  • rs115952495Benignsingle nucleotide variantPrimary ciliary dyskinesia|Primary ciliary dyskinesia 14
  • rs61733578Benignsingle nucleotide variantPrimary ciliary dyskinesia|Primary ciliary dyskinesia 14
  • rs61733583Benignsingle nucleotide variantPrimary ciliary dyskinesia|Primary ciliary dyskinesia 14
  • rs79329972Benignsingle nucleotide variantPrimary ciliary dyskinesia|Primary ciliary dyskinesia 14
  • rs79349285Benignsingle nucleotide variantPrimary ciliary dyskinesia 14
  • rs139560004Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia|Primary ciliary dyskinesia 14
  • rs140505857Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia 14|Primary ciliary dyskinesia
  • rs147383873Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia|Primary ciliary dyskinesia 14
  • rs182803063Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia|Primary ciliary dyskinesia 14
  • rs183413880Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia|Primary ciliary dyskinesia 14
  • rs200089274Conflicting interpretationssingle nucleotide variant
  • rs201684898Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia|Primary ciliary dyskinesia 14
  • rs201780665Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia|Ellis-van Creveld syndrome|Primary ciliary dyskinesia 14
  • rs376737530Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia|Primary ciliary dyskinesia 14
  • rs551191744Conflicting interpretationsDeletionPrimary ciliary dyskinesia|Primary ciliary dyskinesia 14
  • rs769223754Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia
  • rs79353057Conflicting interpretationssingle nucleotide variantPrimary ciliary dyskinesia|Primary ciliary dyskinesia 14

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.