功能: disease:Defects in VCX3A are associated with some forms of X-linked nonspecific mental retardation.,function:May mediate a process in spermatogenesis or may play a role in sex ratio distortion.,similarity:Belongs to the VCX/VCY family.,tissue specificity:Expressed exclusively in testis.,
功能: disease:Defects in VCX3A are associated with some forms of X-linked nonspecific mental retardation.,function:May mediate a process in spermatogenesis or may play a role in sex ratio distortion.,similarity:Belongs to the VCX/VCY family.,tissue specificity:Expressed exclusively in testis.,
相關(guān)產(chǎn)品: RS0001,RS0002,YM3028,YM3029
細(xì)胞定位: nucleus,nucleolus,
組織表達(dá): Expressed exclusively in testis.
科研貨號: PLA020854
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