Gene: CLPB ×
Source: UNIPROT ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 81570
Gene Symbol: CLPB
CLPB 		0.700 GeneticVariation disease UNIPROT CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder. 25597510 2015
Entrez Id: 81570
Gene Symbol: CLPB
CLPB 		0.700 GeneticVariation disease UNIPROT CLPB variants associated with autosomal-recessive mitochondrial disorder with cataract, neutropenia, epilepsy, and methylglutaconic aciduria. 25597511 2015