Microcephaly Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_10907)
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Genes

6 genes associated with the Microcephaly phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
CDK5RAP2 CDK5 regulatory subunit associated protein 2
CENPJ centromere protein J
DPP6 dipeptidyl-peptidase 6
MCPH1 microcephalin 1
MECP2 methyl CpG binding protein 2