Gene: POU5F1P3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 642559
Gene Symbol: POU5F1P3
POU5F1P3 		0.010 PosttranslationalModification disease BEFREE Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome. 24916376 2014