Source: MGD

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1750
Gene Symbol: DLX6
DLX6
CUI: C0265554
Disease: Ectrodactyly
Ectrodactyly 		0.520 Biomarker MGD Regulation of Dlx5 and Dlx6 gene expression by p63 is involved in EEC and SHFM congenital limb defects. 18326838

2008
Entrez Id: 1750
Gene Symbol: DLX6
DLX6
CUI: C0265554
Disease: Ectrodactyly
Ectrodactyly 		0.520 Biomarker MGD Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1. 12112878

2002
Entrez Id: 1750
Gene Symbol: DLX6
DLX6
CUI: C0265554
Disease: Ectrodactyly
Ectrodactyly 		0.520 Biomarker MGD Jaw transformation with gain of symmetry after Dlx5/Dlx6 inactivation: mirror of the past? 12434331

2002