Gene: CCDC88C ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 440193
Gene Symbol: CCDC88C
CCDC88C 		0.310 GeneticVariation disease BEFREE A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia. 25062847 2014
Entrez Id: 440193
Gene Symbol: CCDC88C
CCDC88C 		0.310 Biomarker disease CTD_human