Gene entry
OCLN
occludin
- Chromosome
- 5
- Cytoband
- 5q13.2
- Variants (rsID)
- 8
OCLN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q13.2). Its official name is “occludin”. The reference table lists 8 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs35107257Benignsingle nucleotide variant
- rs28562785Conflicting interpretationssingle nucleotide variantPseudo-TORCH syndrome 1
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.