Gene: CP ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1356
Gene Symbol: CP
CP 		0.130 AlteredExpression group BEFREE This review contributes to better genetic counseling of heterozygotes for CP gene variants and supports that measuring ceruloplasmin levels may be useful when investigating patients with movement disorders or rare cases of unexplained high ferritin. 30901137 2019
Entrez Id: 1356
Gene Symbol: CP
CP 		0.130 GeneticVariation group CLINVAR Aceruloplasminaemia: a family with a novel mutation and long-term therapy with deferasirox. 25089372 2015
Entrez Id: 1356
Gene Symbol: CP
CP 		0.130 GeneticVariation group CLINVAR Aceruloplasminemia: a novel mutation in a family with marked phenotypic variability. 18200628 2008
Entrez Id: 1356
Gene Symbol: CP
CP 		0.130 GeneticVariation group CLINVAR Molecular and pathological basis of aceruloplasminemia. 16629161 2006
Entrez Id: 1356
Gene Symbol: CP
CP 		0.130 GeneticVariation group BEFREE Novel mutation in the ceruloplasmin gene causing a cognitive and movement disorder with diabetes mellitus. 17013908 2006
Entrez Id: 1356
Gene Symbol: CP
CP 		0.130 GeneticVariation group CLINVAR Aceruloplasminemia, an iron metabolic disorder. 14719552 2003
Entrez Id: 1356
Gene Symbol: CP
CP 		0.130 GeneticVariation group BEFREE The clinical and laboratory findings suggest that additional patients with movement disorders and nonclassical Wilson disease should be examined for ceruloplasmin gene mutations. 7708681 1995