High mobility group nucleosomal binding domain 2 pseudogene 36 (HMGN2P36)

HMGN2P36 (high mobility group nucleosomal binding domain 2 pseudogene 36) is a human pseudogene located on chromosome 11 (11:13610363-13610771)[5][10]. As a pseudogene, it is a non-functional genomic DNA sequence that resembles the high mobility group nucleosomal binding domain 2 (HMGN2) gene. Pseudogenes like HMGN2P36 are typically generated by duplication or retrotransposition events involving functional genes, followed by the accumulation of mutations that prevent the formation of a functional protein[2][8][7]. There is currently no evidence for a protein product or conventional gene function for HMGN2P36, nor any established role in disease or therapy. HMGN2P36 is a pseudogene, does not encode a functional protein, and is not a therapeutic target. No known drugs, biomarkers, safety concerns, or disease roles exist for this entry. The designation "target" is inappropriate for HMGN2P36 in the context of molecular pharmacology or drug discovery.

Other names

HMGN2P36100874480 (NCBI Gene ID)