Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 GeneticVariation group CLINVAR Molecular and phenotypic spectrum of ASPM-related primary microcephaly: Identification of eight novel mutations. 27250695 2016
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 CausalMutation group CLINVAR Molecular and phenotypic spectrum of ASPM-related primary microcephaly: Identification of eight novel mutations. 27250695 2016
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 GeneticVariation group CLINVAR Genetic heterogeneity in Pakistani microcephaly families. 22775483 2013
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 CausalMutation group CLINVAR Genetic heterogeneity in Pakistani microcephaly families. 22775483 2013
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 CausalMutation group CLINVAR A clinical and molecular genetic study of 112 Iranian families with primary microcephaly. 20978018 2010
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 GeneticVariation group CLINVAR A clinical and molecular genetic study of 112 Iranian families with primary microcephaly. 20978018 2010
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 CausalMutation group CLINVAR Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations. 19770472 2009
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 CausalMutation group CLINVAR The molecular landscape of ASPM mutations in primary microcephaly. 19028728 2009
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 GeneticVariation group CLINVAR Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family. 19332161 2009
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 GeneticVariation group CLINVAR Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations. 19770472 2009
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 CausalMutation group CLINVAR Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family. 19332161 2009
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 GeneticVariation group CLINVAR The molecular landscape of ASPM mutations in primary microcephaly. 19028728 2009
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 GeneticVariation group CLINVAR Primary microcephaly with ASPM mutation shows simplified cortical gyration with antero-posterior gradient pre- and post-natally. 18452193 2008
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 CausalMutation group CLINVAR Primary microcephaly with ASPM mutation shows simplified cortical gyration with antero-posterior gradient pre- and post-natally. 18452193 2008
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 GeneticVariation group CLINVAR Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings. 15806441 2005
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 CausalMutation group CLINVAR Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings. 15806441 2005
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 CausalMutation group CLINVAR ASPM mutations identified in patients with primary microcephaly and seizures. 16141009 2005
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 GeneticVariation group CLINVAR ASPM mutations identified in patients with primary microcephaly and seizures. 16141009 2005
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 CausalMutation group CLINVAR ASPM is a major determinant of cerebral cortical size. 12355089 2002
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 GeneticVariation group CLINVAR ASPM is a major determinant of cerebral cortical size. 12355089 2002