DIS3L2, DIS3 like 3'-5' exoribonuclease 2, 129563

N. diseases: 91; N. variants: 22
Disease: Congenital chromosomal disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		0.010 Biomarker group BEFREE By selecting focal regions commonly involved in chromosomal anomalies, we identified genes with a possible role in WT development, based on the prior knowledge of their biological relevance, including <i>MYCN, DIS3L2, MIR562</i>, <i>HACE1</i>, <i>GLI3</i>, <i>CDKN2A</i> and <i>CDKN2B</i>, <i>PALB2</i>, and <i>CHEK2</i>. 30344923 2018