Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1749
Gene Symbol: DLX5
DLX5
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.310 Biomarker BEFREE Through genotype-phenotype correlations of 100 patients with molecularly characterized chromosomal aberrations from 32 SHFM1 families, our findings suggest three phenotypic subregions within the SHFM1 locus associated with (1) isolated SHFM, (2) SHFM and hearing loss, and (3) SHFM, hearing loss, and craniofacial anomalies, respectively (ranked for increasing proximity to DLX5/6), and encompassing previously reported tissue-specific enhancers for DLX5/6. 26839112

2016
Entrez Id: 1749
Gene Symbol: DLX5
DLX5
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.310 Biomarker CTD_human Dlx5/6-enhancer directed expression of Cre recombinase in the pharyngeal arches and brain. 14666512

2003
Entrez Id: 1749
Gene Symbol: DLX5
DLX5
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.310 Biomarker CTD_human Dlx5 regulates regional development of the branchial arches and sensory capsules. 10433912

1999
Entrez Id: 1749
Gene Symbol: DLX5
DLX5
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.310 Biomarker CTD_human Craniofacial, vestibular and bone defects in mice lacking the Distal-less-related gene Dlx5. 10433909

1999