Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.700 GermlineCausalMutation disease ORPHANET
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.700 CausalMutation disease CLINVAR
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.700 GeneticVariation disease CLINVAR
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 55755
Gene Symbol: CDK5RAP2
CDK5RAP2
0.690 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 55755
Gene Symbol: CDK5RAP2
CDK5RAP2
0.690 CausalMutation disease CLINVAR
Entrez Id: 55755
Gene Symbol: CDK5RAP2
CDK5RAP2
0.690 GermlineCausalMutation disease ORPHANET
Entrez Id: 79648
Gene Symbol: MCPH1
MCPH1
0.500 CausalMutation disease CLINVAR
Entrez Id: 79648
Gene Symbol: MCPH1
MCPH1
0.500 GermlineCausalMutation disease ORPHANET
Entrez Id: 6491
Gene Symbol: STIL
STIL
0.440 CausalMutation disease CLINVAR
Entrez Id: 6491
Gene Symbol: STIL
STIL
0.440 GermlineCausalMutation disease ORPHANET
Entrez Id: 55835
Gene Symbol: CENPJ
CENPJ
0.430 CausalMutation disease CLINVAR
Entrez Id: 55835
Gene Symbol: CENPJ
CENPJ
0.430 GeneticVariation disease CLINVAR
Entrez Id: 55835
Gene Symbol: CENPJ
CENPJ
0.430 GermlineCausalMutation disease ORPHANET
Entrez Id: 284403
Gene Symbol: WDR62
WDR62
0.400 GermlineCausalMutation disease ORPHANET
Entrez Id: 11113
Gene Symbol: CIT
CIT
0.400 CausalMutation disease CLINVAR
Entrez Id: 22995
Gene Symbol: CEP152
CEP152
0.320 GermlineCausalMutation disease ORPHANET
Entrez Id: 57082
Gene Symbol: KNL1
KNL1
0.320 GermlineCausalMutation disease ORPHANET
Entrez Id: 9662
Gene Symbol: CEP135
CEP135
0.310 GermlineCausalMutation disease ORPHANET
Entrez Id: 80254
Gene Symbol: CEP63
CEP63
0.310 GermlineCausalMutation disease ORPHANET
Entrez Id: 1911
Gene Symbol: PHC1
PHC1
0.300 GermlineCausalMutation disease ORPHANET
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.700 Biomarker disease BEFREE Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32. 11067780 2000
Entrez Id: 79648
Gene Symbol: MCPH1
MCPH1
0.500 GeneticVariation disease BEFREE Autosomal Recessive Primary Microcephaly (MCPH) is one of those, for which seven loci (MCPH1-MCPH7) with the corresponding genes (MCPH1, WDR62, CDK5RAP2, CEP152, ASPM, CENPJ, and STIL) have been reported so far. 24148351 2013
Entrez Id: 6491
Gene Symbol: STIL
STIL
0.440 GeneticVariation disease BEFREE Autosomal Recessive Primary Microcephaly (MCPH) is one of those, for which seven loci (MCPH1-MCPH7) with the corresponding genes (MCPH1, WDR62, CDK5RAP2, CEP152, ASPM, CENPJ, and STIL) have been reported so far. 24148351 2013
Entrez Id: 284403
Gene Symbol: WDR62
WDR62
0.400 GeneticVariation disease BEFREE Autosomal Recessive Primary Microcephaly (MCPH) is one of those, for which seven loci (MCPH1-MCPH7) with the corresponding genes (MCPH1, WDR62, CDK5RAP2, CEP152, ASPM, CENPJ, and STIL) have been reported so far. 24148351 2013