Gene table: search width pubmed_id = 33239111


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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 3 - (AD)
5.24
33239111
NOTCH2NLC (1q21.2)
Notch2 N-terminal-like protein
* Neuronal intranuclear inclusion diseases - NIID
* Oculopharyngodistal myopathy
* Charcot-Marie-Tooth disease, axonal, related to NOTCH2NLC - CMT2