Gene: FNBP4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23360
Gene Symbol: FNBP4
FNBP4 		0.310 GeneticVariation disease BEFREE Whole-exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies. 23703728 2013
Entrez Id: 23360
Gene Symbol: FNBP4
FNBP4 		0.310 Biomarker disease GENOMICS_ENGLAND