Gene entry
PTX3
pentraxin 3
- Chromosome
- 3
- Cytoband
- 3q25.32
- Variants (rsID)
- 3
PTX3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q25.32). Its official name is “pentraxin 3”. The reference table lists 3 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs3816527Not classifiedmissense_variantMigraine with or Without Aura 1|Headache|Chronic Kidney Disease|Kidney Disease|Aspergillosis|Invasive Aspergillosis|Pulmonary Disease, Chronic Obstructive|Allergic Bronchopulmonary Aspergillosis|Cryptococcosis|Fungal Infectious Disease|Oral Cancer|Inflammatory Spondylopathy|Spondyloarthropathy 1|Spondylitis|Coronary Heart Disease 1|Pneumonia|Mycobacterium Tuberculosis 1|Cervical Cancer
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.