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Summary Attributions
Transgene Name Tg(sobpR651X)
Description This construct has an engineered mutation of the Xenopus sobp replicating a human mutation associated with mental retardation, anterior maxillary protrusion, strabismus and mild hearing loss (MRAMS; OMIM #613671). The homozygous variant inserts an early stop codon at arginine 661 (p.R661X), causing a 212 amino acid truncation in the C terminus.
Inducibility None


Name sobp{R651X}
Type ORF from cDNA
Sequence No sequence available
Organism Xenopus laevis

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