Proline-rich protein 23D2 (PRR23D2)

Proline-rich protein 23D2 is a protein-coding gene located on chromosome 8 in humans. It is also known as PRR23D1, and shares high sequence similarity with other proline-rich proteins. The protein is classified as a predicted intracellular protein with unknown molecular function and limited characterization in terms of biology or disease involvement. There is currently no evidence that PRR23D2 serves as a therapeutic target, nor are there any drugs known to interact with it or diseases directly linked to its activity. Expression studies and available databases do not ascribe clear molecular functions, classifications, or therapeutic relevance at this time. There is a similarly named gene, PRRT2 (Proline-rich transmembrane protein 2), which is associated with neurological diseases and well-characterized synaptic functions, but PRR23D2 is a distinct and unrelated gene. Some molecular function listings (such as "acyltransferase" or "non-receptor serine/threonine kinase" from mass annotation databases) are potentially erroneous or generic, and do not reflect consensus or specific functional validation for PRR23D2.

Other names

PRR23D2PRR23D1Proline-rich protein 23D2Proline-rich protein 23D1proline-rich protein 23C-like