Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 27229
Gene Symbol: TUBGCP4
TUBGCP4 		0.600 GeneticVariation disease CLINVAR Mutations in TUBGCP4 alter microtubule organization via the γ-tubulin ring complex in autosomal-recessive microcephaly with chorioretinopathy. 25817018 2015
Entrez Id: 27229
Gene Symbol: TUBGCP4
TUBGCP4 		0.600 GermlineCausalMutation disease ORPHANET Mutations in TUBGCP4 alter microtubule organization via the γ-tubulin ring complex in autosomal-recessive microcephaly with chorioretinopathy. 25817018 2015
Entrez Id: 27229
Gene Symbol: TUBGCP4
TUBGCP4 		0.600 Biomarker disease CTD_human
Entrez Id: 10733
Gene Symbol: PLK4
PLK4 		0.500 GermlineCausalMutation disease ORPHANET Novel compound heterozygous variants in PLK4 identified in a patient with autosomal recessive microcephaly and chorioretinopathy. 27650967 2016
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		0.500 GermlineCausalMutation disease ORPHANET Genetic mapping and exome sequencing identify variants associated with five novel diseases. 22279524 2012
Entrez Id: 85378
Gene Symbol: TUBGCP6
TUBGCP6 		0.500 Biomarker disease CTD_human
Entrez Id: 10733
Gene Symbol: PLK4
PLK4 		0.500 Biomarker disease CTD_human
Entrez Id: 7158
Gene Symbol: TP53BP1
TP53BP1 		0.100 GeneticVariation disease CLINVAR Mutations in TUBGCP4 alter microtubule organization via the γ-tubulin ring complex in autosomal-recessive microcephaly with chorioretinopathy. 25817018 2015