Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2
0.460 Biomarker disease BEFREE Exome sequencing identifies ZFPM2 as a cause of familial isolated congenital diaphragmatic hernia and possibly cardiovascular malformations. 24769157 2015
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2
0.460 GeneticVariation disease BEFREE Findings from the patients described herein indicate that ZFPM2 point mutations or deletions are a recurring cause of CDH. 24702427 2015
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2
0.460 GeneticVariation disease BEFREE Inherited deletions of ZFPM2 were identified in 2 patients with isolated diaphragmatic defects and a large de novo 8q deletion overlapping the same gene was found in a patient with non-isolated CDH. 21525063 2011
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2
0.460 SusceptibilityMutation disease ORPHANET Inherited deletions of ZFPM2 were identified in 2 patients with isolated diaphragmatic defects and a large de novo 8q deletion overlapping the same gene was found in a patient with non-isolated CDH. 21525063 2011
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2
0.460 Biomarker disease BEFREE In two patients (Patients 2 and 4), ZFPM2 (also called FOG2, a candidate gene for congenital diaphragmatic hernias) was partly deleted. 21739578 2011
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2
0.460 Biomarker disease BEFREE The COUP-TFII, FOG2, and GATA4 genes, regulated by the retinoid signaling pathway, are located on chromosomes 15q26, 8q23, and 8p23.1 respectively, regions reported to be deleted in individuals with CDH. 19853750 2009
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2
0.460 GeneticVariation disease BEFREE For FOG2, we identified novel sequence alterations predicting p.M703L and p.T843A in two patients with isolated CDH that were absent in 526 and 564 control chromosomes respectively. 17568391 2007
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2
0.460 Biomarker disease HPO