Gene: SLC25A22 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79751
Gene Symbol: SLC25A22
SLC25A22 		0.120 GeneticVariation disease BEFREE Mutations in SLC25A22 are known to cause neonatal epileptic encephalopathy and migrating partial seizures in infancy. 28255779 2017
Entrez Id: 79751
Gene Symbol: SLC25A22
SLC25A22 		0.120 GeneticVariation disease BEFREE Comparison of the clinical features of patients from both families suggests that SLC25A22 mutations are responsible for a novel clinically recognizable epileptic encephalopathy with SB. 19780765 2009
Entrez Id: 79751
Gene Symbol: SLC25A22
SLC25A22 		0.120 Biomarker disease HPO