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Gene entry

LTBP4

latent transforming growth factor beta binding protein 4

Chromosome
19
Cytoband
19q13.2
Variants (rsID)
27

LTBP4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.2). Its official name is “latent transforming growth factor beta binding protein 4”. The reference table lists 27 variants (rsID) for this gene.

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Clinically classified variants

17 reference-table entries with clinical significance.

  • rs1051303Benignsingle nucleotide variantCutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
  • rs1131620Benignsingle nucleotide variantCutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
  • rs114749335Benignsingle nucleotide variantCutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
  • rs115718556Benignsingle nucleotide variant
  • rs116005784Benignsingle nucleotide variantCutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
  • rs117273116Benignsingle nucleotide variantCutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
  • rs185400394Benignsingle nucleotide variant
  • rs2303729Benignsingle nucleotide variantCutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
  • rs34093919Benignsingle nucleotide variantCutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
  • rs34299942Benignsingle nucleotide variantCutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
  • rs35079932Benignsingle nucleotide variant
  • rs35809725Benignsingle nucleotide variant
  • rs370696272Benignsingle nucleotide variantCutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
  • rs73544980Benignsingle nucleotide variantCutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
  • rs7367Benignsingle nucleotide variantCutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
  • rs78745792Benignsingle nucleotide variant
  • rs148592974Likely benignsingle nucleotide variant

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.