Gene: HMGN2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3151
Gene Symbol: HMGN2
HMGN2 		0.010 AlteredExpression disease BEFREE Here, we show that a mouse model with deficient expression of high mobility group nucleosomal binding domain 2 (HMGN2) manifests microcephaly with reduced cortical surface area and almost normal radial corticogenesis, with a pattern of incomplete penetrance. 31699896 2020