TR150 Polyclonal Antibody, 50ul Antibodies Mutations in this gene cause

Mutations in this gene cause a form of retinitis pigmentosa characterized by autosomal recessive cone and rod dystrophy (arCRD)

GO annotations related to this gene include poly (A) RNA binding and protein kinase activity

tissue specificity:Ubiquitously expressed with higher expression found in heart and placenta

its official symbol is RPL23

This gene encodes a specific phosphotyrosyl phosphatase activator of the dimeric form of protein phosphatase 2A

TR150 Polyclonal Antibody, 50ul Antibodies Mutations in this gene causePlays a role in transcriptional coactivation.,PTM: Phosphorylated upon DNA damage, probably by ATM or ATR.,sequence Contaminating sequence. Potential poly A sequence.,subunit: Subunit of the large multiprotein complex TRAP.,tissue specificity: Ubiquitous.,