Gene entry
TGM5
transglutaminase 5
- Chromosome
- 15
- Cytoband
- 15q15.2
- Variants (rsID)
- 19
TGM5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q15.2). Its official name is “transglutaminase 5”. The reference table lists 19 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs35985214Benignsingle nucleotide variantAcral peeling skin syndrome
- rs61744878Benignsingle nucleotide variantAcral peeling skin syndrome
- rs112292549Pathogenicsingle nucleotide variantAcral peeling skin syndrome|Inborn genetic diseases
- rs115677373Pathogenicsingle nucleotide variantAcral peeling skin syndrome
- rs143601447Uncertain significancesingle nucleotide variantAcral peeling skin syndrome
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.