Gene: NOP56 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10528
Gene Symbol: NOP56
NOP56 		0.020 Biomarker group BEFREE In particular, SCA36 is characterized by a late-onset, slowly progressive cerebellar syndrome typically associated with sensorineural hearing loss. 27862279 2017
Entrez Id: 10528
Gene Symbol: NOP56
NOP56 		0.020 GeneticVariation group BEFREE Spinocerebellar ataxia type 36 is a late-onset, slowly progressive cerebellar syndrome with motor neuron degeneration that is caused by expansions of a hexanucleotide repeat (GGCCTG) in the noncoding region of NOP56 gene, with a histopathological feature of RNA foci formation in postmortem tissues. 28918022 2017