Gene table: search width pubmed_id = 34675106


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

protein
All allelic disease phenotypes - locus/disease symbols
Charcot-Marie-Tooth disease, axonal, related to NOTCH2NLC - (AD)
14.84
34675106
NOTCH2NLC (1q21.2)
Notch2 N-terminal-like protein
* Neuronal intranuclear inclusion diseases - NIID
* Oculopharyngodistal myopathy
* Charcot-Marie-Tooth disease, axonal, related to NOTCH2NLC - CMT2