PRTFDC1 (phosphoribosyl transferase domain containing 1) is a protein-coding gene. Diseases associated with PRTFDC1 include lesch-nyhan syndrome, and oral squamous cell carcinoma. GO annotations related to this gene include magnesium ion binding and protein homodimerization activity. An important paralog of this gene is HPRT1.
Custom Antibody Labeling
We offer labeled antibodies using our catalogue antibody products and a broad range of intensely fluorescent dyes and labels including HRP, biotin, ALP, Alexa Fluor® dyes, DyLight® Fluor dyes, R-phycoerythrin (R-PE), at scales from less than 100 μg up to 1 g of IgG antibody. Learn More
Citations
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Keebaugh, AC; Sullivan, RT; et al. Gene duplication and inactivation in the HPRT gene family. GENOMICS 89:134-142(2007).
Nievergelt, CM; Maihofer, AX; et al. Genomic predictors of combat stress vulnerability and resilience in US Marines: A genome-wide association study across multiple ancestries implicates PRTFDC1 as a potential PTSD gene. PSYCHONEUROENDOCRINOLOGY 51:459-471(2015).
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