Gene: C12orf65 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 91574
Gene Symbol: C12orf65
C12orf65 		0.010 Biomarker group BEFREE Some reported cases have been found to carry mutations in the OPA1, OPA3 or C12ORF65 genes which are known causes of pure optic atrophy or optic atrophy complicated by movement disorder. 26187298 2015