Gene: ALX4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 60529
Gene Symbol: ALX4
ALX4 		0.100 CausalMutation group CLINVAR ALX4 gain-of-function mutations in nonsyndromic craniosynostosis. 22829454 2012
Entrez Id: 60529
Gene Symbol: ALX4
ALX4 		0.100 CausalMutation group CLINVAR ALX4 dysfunction disrupts craniofacial and epidermal development. 19692347 2009
Entrez Id: 60529
Gene Symbol: ALX4
ALX4 		0.100 CausalMutation group CLINVAR Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype. 16319823 2006
Entrez Id: 60529
Gene Symbol: ALX4
ALX4 		0.100 CausalMutation group CLINVAR Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects. 11137991 2001
Entrez Id: 60529
Gene Symbol: ALX4
ALX4 		0.100 CausalMutation group CLINVAR The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). 11106354 2000
Entrez Id: 60529
Gene Symbol: ALX4
ALX4 		0.100 CausalMutation group CLINVAR Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome. 11017806 2000