VCX3 Rabbit Polyclonal Antibody, 50ul Centrifugal Filter retinitis pigmentosa

retinitis pigmentosa

Mutations in this gene have been associated with autosomal mental retardation-39 and autism spectrum disorder

EPHB6 encodes a member of a family of transmembrane proteins that function as receptors for ephrin-B family proteins

It is also expressed in embryonic and adult olfactory neuroepithelia where it complexes with eukaryotic translation initiation factor 4E (eIF4E) and possibly regulates mRNA transport or translation

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VCX3 Rabbit Polyclonal Antibody, 50ul Centrifugal Filter retinitis pigmentosaThis gene belongs to the VCX Y gene family which has multiple members on both X and Y chromosomes and all are expressed exclusively in male germ cells. The X linked members are clustered on chromosome Xp22 and Y linked members are two identical copies of the gene within a palindromic region on Yq11. The family members share a high degree of sequence identity with the exception that a 30 bp unit is tandemly repeated in X linked members but occurs only