WD repeat-containing protein 62 (IPR030545)

Short name: WDR62

Family relationships



The function of WD repeat domain 62 (WDR62) is not clear. Human WDR62 localises at centrosomes [PMID: 21496009]. It plays a role in many aspects of cerebral cortical development [PMID: 20890278]. Mutations in WDR62 cause a wide spectrum of severe cerebral cortical malformations including microcephaly, pachygyria with cortical thickening as well as hypoplasia of the corpus callosum [PMID: 20729831].

Contributing signatures

Signatures from InterPro member databases are used to construct an entry.