FTSJ1 (FtsJ RNA methyltransferase homolog 1 (E. coli)) is a protein-coding gene. Diseases associated with FTSJ1 include fryns syndrome, and mental retardation, x-linked. GO annotations related to this gene include methyltransferase activity.
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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Ramser, J; Winnepenninckx, B; et al. A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9). JOURNAL OF MEDICAL GENETICS 41:679-683(2004).
Bonnet, C; Gregoire, MJ; et al. Pure de-novo 5 Mb duplication at Xp11.22-p11.23 in a male: phenotypic and molecular characterization. JOURNAL OF HUMAN GENETICS 51:815-821(2006).
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