Gene: CYP2U1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 113612
Gene Symbol: CYP2U1
CYP2U1 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis. 24337409 2014
Entrez Id: 113612
Gene Symbol: CYP2U1
CYP2U1 		0.700 GermlineCausalMutation disease ORPHANET Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia. 23176821 2012
Entrez Id: 113612
Gene Symbol: CYP2U1
CYP2U1 		0.700 GeneticVariation disease UNIPROT Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia. 23176821 2012
Entrez Id: 113612
Gene Symbol: CYP2U1
CYP2U1 		0.700 CausalMutation disease CLINVAR Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia. 23176821 2012
Entrez Id: 113612
Gene Symbol: CYP2U1
CYP2U1 		0.700 Biomarker disease GENOMICS_ENGLAND Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia. 23176821 2012
Entrez Id: 113612
Gene Symbol: CYP2U1
CYP2U1 		0.700 GeneticVariation disease CLINVAR
Entrez Id: 113612
Gene Symbol: CYP2U1
CYP2U1 		0.700 Biomarker disease CTD_human
Entrez Id: 113612
Gene Symbol: CYP2U1
CYP2U1 		0.700 Biomarker disease GENOMICS_ENGLAND