Gene: ASXL2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55252
Gene Symbol: ASXL2
ASXL2 		0.110 Biomarker disease BEFREE Although overlapping features with Bohring-Opitz and Bainbridge-Ropers syndromes exist, features that distinguish the ASXL2-associated condition from ASXL1- and ASXL3-related disorders are macrocephaly, absence of growth retardation, and more variability in the degree of intellectual disabilities. 27693232 2016
Entrez Id: 55252
Gene Symbol: ASXL2
ASXL2 		0.110 Biomarker disease HPO