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 		0.610 Biomarker disease GENOMICS_ENGLAND Identification of FASTKD2 compound heterozygous mutations as the underlying cause of autosomal recessive MELAS-like syndrome. 28499982 2017
Entrez Id: 22868
Gene Symbol: FASTKD2
FASTKD2 		0.610 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 22868
Gene Symbol: FASTKD2
FASTKD2 		0.610 GeneticVariation disease BEFREE FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency. 18771761 2008
Entrez Id: 22868
Gene Symbol: FASTKD2
FASTKD2 		0.610 CausalMutation disease CLINVAR
Entrez Id: 22868
Gene Symbol: FASTKD2
FASTKD2 		0.610 Biomarker disease CTD_human
Entrez Id: 22868
Gene Symbol: FASTKD2
FASTKD2 		0.610 Biomarker disease GENOMICS_ENGLAND