Gene entry
CTSF
cathepsin F
- Chromosome
- 11
- Cytoband
- 11q13.2
- Variants (rsID)
- 3
CTSF is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q13.2). Its official name is “cathepsin F”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs143313688Conflicting interpretationssingle nucleotide variantSeizure|Neuronal ceroid lipofuscinosis 13
- rs148611356Conflicting interpretationssingle nucleotide variantSeizure|Neuronal ceroid lipofuscinosis 13
- rs141915593Likely pathogenicsingle nucleotide variantNeuronal ceroid lipofuscinosis 13
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.