Gene table: search width pubmed_id = 32413282


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
Oculopharyngodistal myopathy 2 - (AD)
5.23
32413282
GIPC1 (19p13.12)
GIPC PDZ Domain-containing family, member 1
* Oculopharyngodistal myopathy 2 - OPDM2