CDX1, caudal type homeobox 1, 1044

N. diseases: 54; N. variants: 1
Disease: Childhood Mesenchymal Chondrosarcoma ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1332982
Disease: Childhood Mesenchymal Chondrosarcoma
Childhood Mesenchymal Chondrosarcoma 		0.010 GeneticVariation disease BEFREE Whole-transcriptome sequencing identifies novel IRF2BP2-CDX1 fusion gene brought about by translocation t(1;5)(q42;q32) in mesenchymal chondrosarcoma. 23185413 2012