Gene table: search width pubmed_id = 39068203


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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 5 - (AD)
5.27
39068203
ABCD3 (1p21.3)
ATP-binding cassette, subfamily D, member 3
* Oculopharyngodistal myopathy 5 - OPDM5