Also known as HEL-S-92n, PTX2, SAP, amyloid P component, serum
protein-coding gene in the species Homo sapiens
The protein encoded by this gene is a glycoprotein, belonging to the pentraxin family of proteins, which has a characteristic pentameric organization. These family members have considerable sequence homology which is thought to be the result of gene duplication. The binding of the encoded protein to proteins in the pathological amyloid cross-beta fold suggests its possible role as a chaperone. This protein is also thought to control the degradation of chromatin. It has been demonstrated that this protein binds to apoptotic cells at an early stage, which raises the possibility that it is involved in dealing with apoptotic cells in vivo. [provided by RefSeq, Sep 2008].
via MyGene.info
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Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).