Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79823
Gene Symbol: CAMKMT
CAMKMT
0.300 Biomarker disease CTD_human Calmodulin Methyltransferase Is Required for Growth, Muscle Strength, Somatosensory Development and Brain Function. 26247364 2015
Entrez Id: 50484
Gene Symbol: RRM2B
RRM2B
0.300 Biomarker disease CTD_human A novel homozygous RRM2B missense mutation in association with severe mtDNA depletion. 19138848 2009
Entrez Id: 50484
Gene Symbol: RRM2B
RRM2B
0.300 Biomarker disease CTD_human Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion. 17486094 2007
Entrez Id: 7416
Gene Symbol: VDAC1
VDAC1
0.300 Biomarker disease CTD_human Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathy. 8726225 1996
Entrez Id: 3553
Gene Symbol: IL1B
IL1B
0.300 Biomarker disease CTD_human Cytokine expression in the muscle of HIV-infected patients: evidence for interleukin-1 alpha accumulation in mitochondria of AZT fibers. 7979221 1994
Entrez Id: 3569
Gene Symbol: IL6
IL6
0.300 Biomarker disease CTD_human Cytokine expression in the muscle of HIV-infected patients: evidence for interleukin-1 alpha accumulation in mitochondria of AZT fibers. 7979221 1994
Entrez Id: 3552
Gene Symbol: IL1A
IL1A
0.300 Biomarker disease CTD_human Cytokine expression in the muscle of HIV-infected patients: evidence for interleukin-1 alpha accumulation in mitochondria of AZT fibers. 7979221 1994
Entrez Id: 7124
Gene Symbol: TNF
TNF
0.300 Biomarker disease CTD_human Cytokine expression in the muscle of HIV-infected patients: evidence for interleukin-1 alpha accumulation in mitochondria of AZT fibers. 7979221 1994
Entrez Id: 112812
Gene Symbol: FDX2
FDX2
0.300 Biomarker disease CTD_human
Entrez Id: 4578
Gene Symbol: TRNW
TRNW
0.300 Biomarker disease CTD_human
Entrez Id: 1120
Gene Symbol: CHKB
CHKB
0.010 GeneticVariation disease BEFREE Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene. 26006750 2016