RGD Annotation Report for Spinocerebellar AtaxiasRat Genome Database

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An association has been curated linking Nop56 and Spinocerebellar Ataxias in Rattus norvegicus.

The association was inferred from sequence orthology (ISO)
The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
The annotation has been inferred from sequence orthology with NOP56 (Homo sapiens) [(EXP) inferred from experiment]
555 RGD objects have been annotated to Spinocerebellar Ataxias (DOID:9002121)
7 papers in RGD have been used to annotate Nop56
Curation Notes: CTD Direct Evidence: marker/mechanism

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.