Gene entry
KRT9
keratin 9
- Chromosome
- 17
- Cytoband
- 17q21.2
- Variants (rsID)
- 6
KRT9 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 9”. The reference table lists 6 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs77688767Conflicting interpretationssingle nucleotide variantEpidermolytic palmoplantar keratoderma
- rs56707768Pathogenicsingle nucleotide variantEpidermolytic palmoplantar keratoderma
- rs59616921Pathogenicsingle nucleotide variantPalmoplantar keratoderma, epidermolytic, with knuckle pads|Epidermolytic palmoplantar keratoderma|Palmoplantar keratoderma
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.