wdr62
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  • Official Full Name
  • WD repeat domain 62
  • Background
  • This gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly, cortical malformations, and mental retardation. Alternative splicing results in multiple transcript variants.
  • Synonyms
  • WDR62; WD repeat domain 62; C19orf14, chromosome 19 open reading frame 14 , MCPH2, microcephaly, primary autosomal recessive 2; WD repeat-containing protein 62; DKFZP434J046; FLJ33298; C19orf14; Chromosome 19 open reading frame 14; MGC166976; microcephaly, primary autosomal recessive 2; MCPH2