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Intellectual_disability

Gene: ASPM

Red List (low evidence)

ASPM (abnormal spindle microtubule assembly)
EnsemblGeneIds (GRCh38): ENSG00000066279
EnsemblGeneIds (GRCh37): ENSG00000066279
OMIM: 605481, Gene2Phenotype
ASPM is in 5 panels

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Details

Sources
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Microcephaly 5, primary, autosomal recessive, 608716
OMIM
605481
Clinvar variants
Variants in ASPM
Penetrance
Complete
Panels with this gene

History Filter Activity

8 Oct 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

ASPM was added to Intellectual_disabilitypanel. Sources: Radboud University Medical Center, Nijmegen