GOLGA2, golgin A2, 2801

N. diseases: 29; N. variants: 3
Disease: Cerebellar Ataxia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		0.010 Biomarker phenotype BEFREE Loss of the golgin GM130 causes Golgi disruption, Purkinje neuron loss, and ataxia in mice. 28028212 2017