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Gene entry

CRTAP

cartilage associated protein

Chromosome
3
Cytoband
3p22.3
Variants (rsID)
14

CRTAP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p22.3). Its official name is “cartilage associated protein”. The reference table lists 14 variants (rsID) for this gene.

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Clinically classified variants

6 reference-table entries with clinical significance.

  • rs4076086Benignsingle nucleotide variantOsteogenesis imperfecta type 7
  • rs4355234Benignsingle nucleotide variantOsteogenesis imperfecta type 7
  • rs115198029Conflicting interpretationssingle nucleotide variantOsteogenesis imperfecta type 7|Osteogenesis imperfecta
  • rs149119710Conflicting interpretationssingle nucleotide variantOsteogenesis imperfecta type 7|Osteogenesis imperfecta
  • rs201267683Uncertain significancesingle nucleotide variantOsteogenesis imperfecta type 7|Osteogenesis imperfecta
  • rs202118861Uncertain significancesingle nucleotide variantOsteogenesis imperfecta type 7|Osteogenesis imperfecta

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.