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Gene entry

TRIP11

thyroid hormone receptor interactor 11

Chromosome
14
Cytoband
14q32.12
Variants (rsID)
18

TRIP11 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q32.12). Its official name is “thyroid hormone receptor interactor 11”. The reference table lists 18 variants (rsID) for this gene.

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Clinically classified variants

11 reference-table entries with clinical significance.

  • rs117748213Benignsingle nucleotide variantAchondrogenesis, type IA|Connective tissue disorder
  • rs141965887Benignsingle nucleotide variantAchondrogenesis, type IA|Connective tissue disorder
  • rs143524436Benignsingle nucleotide variantAchondrogenesis, type IA|Connective tissue disorder
  • rs2273186Benignsingle nucleotide variantAchondrogenesis, type IA|Connective tissue disorder
  • rs35007347Benignsingle nucleotide variantAchondrogenesis, type IA|Connective tissue disorder
  • rs74071672Benignsingle nucleotide variantAchondrogenesis, type IA|Connective tissue disorder
  • rs139539448Conflicting interpretationssingle nucleotide variantAchondrogenesis, type IA|Connective tissue disorder
  • rs141259390Conflicting interpretationssingle nucleotide variantAchondrogenesis, type IA|Connective tissue disorder
  • rs148261539Conflicting interpretationssingle nucleotide variantAchondrogenesis, type IA|Connective tissue disorder
  • rs41301481Conflicting interpretationssingle nucleotide variantAchondrogenesis, type IA|Connective tissue disorder
  • rs137938779Uncertain significancesingle nucleotide variantAchondrogenesis, type IA

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.