Gene: FASTKD2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 22868
Gene Symbol: FASTKD2
FASTKD2 		0.020 GeneticVariation disease BEFREE A FASTKD2 nonsense mutation was once reported as the cause of a recessive infantile mitochondrial encephalomyopathy. 28499982 2017
Entrez Id: 22868
Gene Symbol: FASTKD2
FASTKD2 		0.020 GeneticVariation disease LHGDN FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency. 18771761 2008
Entrez Id: 22868
Gene Symbol: FASTKD2
FASTKD2 		0.020 GeneticVariation disease BEFREE FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency. 18771761 2008