Gene entry
SPINK5
serine peptidase inhibitor Kazal type 5
- Chromosome
- 5
- Cytoband
- 5q32
- Variants (rsID)
- 28
SPINK5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q32). Its official name is “serine peptidase inhibitor Kazal type 5”. The reference table lists 28 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs115504632Benignsingle nucleotide variantNetherton syndrome
- rs17705005Benignsingle nucleotide variantNetherton syndrome
- rs17860502Benignsingle nucleotide variantNetherton syndrome
- rs2303070Benignsingle nucleotide variantNetherton syndrome
- rs28408445Benignsingle nucleotide variantNetherton syndrome
- rs6892205Benignsingle nucleotide variantNetherton syndrome
- rs78128189Benignsingle nucleotide variantNetherton syndrome
- rs368134354Pathogenicsingle nucleotide variantIncreased circulating IgE level|Erythroderma|Netherton 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.
