Gene: CEP135 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9662
Gene Symbol: CEP135
CEP135 		0.310 GeneticVariation disease BEFREE A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function. 22521416 2012
Entrez Id: 9662
Gene Symbol: CEP135
CEP135 		0.310 Biomarker disease GENOMICS_ENGLAND