USP7, ubiquitin specific peptidase 7, 7874

N. diseases: 153; N. variants: 7
Disease: CHROMOSOME 16p13.2 DELETION SYNDROME ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4225667
Disease: CHROMOSOME 16p13.2 DELETION SYNDROME
CHROMOSOME 16p13.2 DELETION SYNDROME 		0.300 ChromosomalRearrangement disease ORPHANET USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder. 26365382 2015