Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 60529
Gene Symbol: ALX4
ALX4
0.420 Biomarker disease BEFREE Only a small number of genes have been associated with FND phenotypes until now, the first gene being EFNB1, related to craniofrontonasal syndrome (CFNS) with craniosynostosis in addition, and more recently the aristaless-like homeobox genes ALX3, ALX4, and ALX1, which have been related with distinct phenotypes named FND1, FND2, and FND3 respectively. 24376213 2014
Entrez Id: 60529
Gene Symbol: ALX4
ALX4
0.420 GeneticVariation disease BEFREE By direct sequencing of the ALX4 coding region in sagittal or sagittal-suture-involved nonsyndromic craniosynostosis probands, we identified novel, nonsynonymous, familial variants in three of 203 individuals with NSC. 22829454 2012
Entrez Id: 60529
Gene Symbol: ALX4
ALX4
0.420 Biomarker disease HPO
Entrez Id: 60529
Gene Symbol: ALX4
ALX4
0.420 Biomarker disease CTD_human