Gene table: search width pubmed_id = 31178126


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Neuronal intranuclear inclusion diseases - (AD)
14.137
31178126
31332380
31332381
NOTCH2NLC (1q21.2)
Notch2 N-terminal-like protein
* Neuronal intranuclear inclusion diseases - NIID
* Oculopharyngodistal myopathy
* Charcot-Marie-Tooth disease, axonal, related to NOTCH2NLC - CMT2