Gene entry
KRT10
keratin 10
- Chromosome
- 17
- Cytoband
- 17q21.2
- Variants (rsID)
- 5
KRT10 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 10”. The reference table lists 5 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs77919366Benignsingle nucleotide variant
- rs58075662Pathogenicsingle nucleotide variantBullous ichthyosiform erythroderma
- rs58852768Pathogenicsingle nucleotide variantBullous ichthyosiform erythroderma|Annular epidermolytic ichthyosis|Congenital reticular ichthyosiform erythroderma|Bullous ichthyosiform erythroderma|Epidermolytic acanthoma
- rs58901407Pathogenicsingle nucleotide variantBullous ichthyosiform erythroderma
- rs59175042Pathogenicsingle nucleotide variant
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.