Gene table: search width pubmed_id = 38159879


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Oculopharyngodistal myopathy - (AD)
5.27
38159879
NUTM2B-AS1 (10q22.3)
NUTM2B antisens RNA 1
* Oculopharyngeal myopathy with leukoencephalopathy 1 - OPML1
* Oculopharyngodistal myopathy