Gene entry
KRT17
keratin 17
- Chromosome
- 17
- Cytoband
- 17q21.2
- Variants (rsID)
- 8
KRT17 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q21.2). Its official name is “keratin 17”. The reference table lists 8 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs121912478PathogenicMicrosatellitePachyonychia congenita 2
- rs28928896Pathogenicsingle nucleotide variantPachyonychia congenita 2
- rs28928899Pathogenicsingle nucleotide variantPachyonychia congenita 2
- rs58730926Pathogenicsingle nucleotide variantSteatocystoma multiplex|Pachyonychia congenita 2
- rs59151893Pathogenicsingle nucleotide variantPachyonychia congenita 2|Abnormality of the skin
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.