×
Entrez Id: 51204
Gene Symbol: TACO1
TACO1
0.300
Biomarker
group
GENOMICS_ENGLAND
×
Entrez Id: 4719
Gene Symbol: NDUFS1
NDUFS1
0.300
Biomarker
group
GENOMICS_ENGLAND
×
Entrez Id: 1327
Gene Symbol: COX4I1
COX4I1
0.300
Biomarker
group
GENOMICS_ENGLAND
×
Entrez Id: 4722
Gene Symbol: NDUFS3
NDUFS3
0.300
Biomarker
group
GENOMICS_ENGLAND
×
Entrez Id: 1340
Gene Symbol: COX6B1
COX6B1
0.300
Biomarker
group
GENOMICS_ENGLAND
×
Entrez Id: 374291
Gene Symbol: NDUFS7
NDUFS7
0.300
Biomarker
group
GENOMICS_ENGLAND
×
Entrez Id: 7386
Gene Symbol: UQCRFS1
UQCRFS1
0.200
Biomarker
group
MGD
×
Entrez Id: 4508
Gene Symbol: ATP6
ATP6
0.180
CausalMutation
group
CLINVAR
×
Entrez Id: 291
Gene Symbol: SLC25A4
SLC25A4
0.140
CausalMutation
group
CLINVAR
×
Entrez Id: 4513
Gene Symbol: COX2
COX2
0.120
CausalMutation
group
CLINVAR
×
Entrez Id: 4566
Gene Symbol: TRNK
TRNK
0.120
CausalMutation
group
CLINVAR
×
Entrez Id: 91689
Gene Symbol: SMDT1
SMDT1
0.100
CausalMutation
group
CLINVAR
×
Entrez Id: 4540
Gene Symbol: ND5
ND5
0.100
CausalMutation
group
CLINVAR
×
Entrez Id: 4700
Gene Symbol: NDUFA6
NDUFA6
0.100
CausalMutation
group
CLINVAR
×
Entrez Id: 4540
Gene Symbol: ND5
ND5
0.100
GeneticVariation
group
CLINVAR
×
Entrez Id: 4538
Gene Symbol: ND4
ND4
0.100
GeneticVariation
group
CLINVAR
×
Entrez Id: 4556
Gene Symbol: TRNE
TRNE
0.100
CausalMutation
group
CLINVAR
×
Entrez Id: 4568
Gene Symbol: TRNL2
TRNL2
0.100
CausalMutation
group
CLINVAR
×
Entrez Id: 56997
Gene Symbol: COQ8A
COQ8A
0.100
GeneticVariation
group
CLINVAR
×
Entrez Id: 4694
Gene Symbol: NDUFA1
NDUFA1
0.330
Biomarker
group
BEFREE
Molecular defects of NADH-ubiquinone oxidoreductase (complex I ) in mitochondrial diseases .
3136150 1988
×
Entrez Id: 4576
Gene Symbol: TRNT
TRNT
0.110
CausalMutation
group
CLINVAR
Mitochondrial disorder associated with newborn cardiopulmonary arrest.
8511015 1993
×
Entrez Id: 4899
Gene Symbol: NRF1
NRF1
0.010
Biomarker
group
BEFREE
These analyses should be useful in evaluating the potential role of NRF-1 in mitochondrial diseases resulting from defects in the nuclear control of mitochondrial function.
7629110 1995
×
Entrez Id: 217
Gene Symbol: ALDH2
ALDH2
0.010
GeneticVariation
group
BEFREE
Thus, this association of ALDH2 genotype with DM-Mt3243 provides insight into the etiology of diabetes in the mitochondrial diseases .
8941476 1996
×
Entrez Id: 2395
Gene Symbol: FXN
FXN
0.090
Biomarker
group
BEFREE
Mutated frataxin triggers aconitase and mitochondrial Fe-S respiratory enzyme deficiency in FRDA, which should therefore be regarded as a mitochondrial disorder .
9326946 1997
×
Entrez Id: 1371
Gene Symbol: CPOX
CPOX
0.040
GeneticVariation
group
BEFREE
A generalized defect of complex IV (cytochrome C oxidase, COX ) is frequently found in subacute necrotizing encephalomyelopathy (Leigh's syndrome), the most common mitochondrial disorder in infancy.
9063742 1997