https://pubchem.ncbi.nlm.nih.gov/gene/NUTM2B
NUTM2B (human) | Gene Target - PubChem
Gene target information for NUTM2B - NUT family member 2B (human). Find diseases associated with this biological target and compounds tested against it in...
human genetargetpubchem
https://blogs.bmj.com/jmg/2023/11/05/non-coding-cgg-repeat-expansion-in-loc642361-nutm2b-as1-is-associated-with-a-phenotype-of-oculopharyngodistal-myopathy/
Non-coding CGG repeat expansion in LOC642361/NUTM2B-AS1 is associated with a phenotype of...
Feb 22, 2026 - Oculopharyngodistal myopathy (OPDM) is a rare neuromuscular disease characterized by progressive ptosis, ophthalmoparesis, facial/bulbar and distal weakness....