Gene: ACSL4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2182
Gene Symbol: ACSL4
ACSL4 		0.710 GeneticVariation disease BEFREE A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients. 12525535 2003
Entrez Id: 2182
Gene Symbol: ACSL4
ACSL4 		0.710 Biomarker disease GENOMICS_ENGLAND FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation. 11889465 2002
Entrez Id: 2182
Gene Symbol: ACSL4
ACSL4 		0.710 GeneticVariation disease UNIPROT FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation. 11889465 2002
Entrez Id: 2182
Gene Symbol: ACSL4
ACSL4 		0.710 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 2182
Gene Symbol: ACSL4
ACSL4 		0.710 Biomarker disease CTD_human
Entrez Id: 2182
Gene Symbol: ACSL4
ACSL4 		0.710 CausalMutation disease CLINVAR