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PMS1 homolog 2, mismatch repair system component pseudogene 7 (PMS2P7)
- Target
- PMS2P7
- Molecular classification
- Other (Pseudogene)
01
Overview
PMS2P7 (PMS1 homolog 2, mismatch repair system component pseudogene 7) is a human pseudogene located in a region with multiple PMS2-related pseudogenes (chromosome bands 7p22, 7p12-p13, 7q11, and 7q22). It was previously annotated as PMS2L15 and PMSR7. Unlike the functional PMS2 gene that encodes a DNA mismatch repair protein associated with Lynch syndrome and other pathologies, PMS2P7 does not produce a functional protein and is generally not implicated in biological processes or disease. As a pseudogene, it neither serves as a drug target nor confers a mechanism of action or safety profile relevant to therapeutic intervention.
- Other names
- PMS2L15PMS2LP2PMS2P7PMSR7Postmeiotic Segregation Increased 2 Pseudogene 7Postmeiotic Segregation Increased 2-Like 15Postmeiotic Segregation Increased 2-Like Pseudogene 2
02
Mechanism of action
No mechanism of action attributable to drugs, as the pseudogene does not encode functional protein
03
Biological functions
No known function; pseudogene
04
Disease associations
Not implicated in disease; does not encode active protein or participate in known pathological mechanisms
05
Safety considerations
No safety concerns or therapeutic challenges as it is not a therapeutic target
06
Interacting drugs
No known drug interactions; not targeted in therapy
07
Biomarkers
No confirmed use as a biomarker for disease, patient selection, or efficacy monitoring in public resources
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