|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|
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WDR62 involved in several pathways and played different roles in them. We selected most pathways WDR62 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with WDR62 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
|Pathway Name||Pathway Related Protein|
WDR62 has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by WDR62 itself. We selected most functions WDR62 had, and list some proteins which have the same functions with WDR62. You can find most of the proteins on our site.
WDR62 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with WDR62 here. Most of them are supplied by our site. Hope this information will be useful for your research of WDR62.