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Gene entry

IFITM5

interferon induced transmembrane protein 5

Chromosome
11
Cytoband
11p15.5
Variants (rsID)
5

IFITM5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p15.5). Its official name is “interferon induced transmembrane protein 5”. The reference table lists 5 variants (rsID) for this gene.

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs141240817Benignsingle nucleotide variant
  • rs786201032Pathogenicsingle nucleotide variantOsteogenesis imperfecta type 5

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.