Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55572
Gene Symbol: FOXRED1
FOXRED1
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19
0.600 GeneticVariation UNIPROT Characterization of mitochondrial FOXRED1 in the assembly of respiratory chain complex I. 25678554

2015

Entrez Id: 55572
Gene Symbol: FOXRED1
FOXRED1
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19
0.600 GeneticVariation UNIPROT High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. 20818383

2010

Entrez Id: 55572
Gene Symbol: FOXRED1
FOXRED1
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19
0.600 GeneticVariation UNIPROT FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy. 20858599

2010