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QuickView for Wdr62 (gene)

Gene Symbol:
WDR62 Homo sapiens Homo sapiens
Full name:
WD repeat domain 62
C19orf14, MCPH2, WD repeat-containing protein 62, microcephaly, primary autosomal recessive 2, truncated WDR62
Genomic Location:
Chr 19: 41237623-41287852
This gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly, cortical malformations, and cognitive disability. Alternative splicing results in multiple transcript variants.
Mus musculus Rattus norvegicus Macaca mulatta Pan troglodytes Canis lupus familiaris Bos taurus Danio rerio
External Links:
Entrez Gene
Transcription Factor
Binding Sites:
miRNA binding sites
(Source: TargetScan):
Cytogenetic Map:
chr 19