merrf syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_310)
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Genes

26 genes co-occuring with the disease merrf syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TK2 thymidine kinase 2, mitochondrial 1.9328
DARS2 aspartyl-tRNA synthetase 2, mitochondrial 1.20959
NPTX2 neuronal pentraxin II 1.09797
TFAM transcription factor A, mitochondrial 1.06396
C10ORF2 chromosome 10 open reading frame 2 1.02229
PFKFB3 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 0.942027
GDAP1 ganglioside induced differentiation associated protein 1 0.869596
VDAC1 voltage-dependent anion channel 1 0.867959
CA8 carbonic anhydrase VIII 0.700321
PHB prohibitin 0.684292
HK2 hexokinase 2 0.640645
ACO2 aconitase 2, mitochondrial 0.624143
MFN2 mitofusin 2 0.6214
POLG polymerase (DNA directed), gamma 0.553239
MMP1 matrix metallopeptidase 1 0.525746
PFKM phosphofructokinase, muscle 0.487407
MAP4 microtubule-associated protein 4 0.465416
AHSG alpha-2-HS-glycoprotein 0.452962
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) 0.388538
GPX1 glutathione peroxidase 1 0.378143
MMP14 matrix metallopeptidase 14 (membrane-inserted) 0.370737
MAP2 microtubule-associated protein 2 0.347511
CAT catalase 0.312102
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1 0.277227
TNFSF10 tumor necrosis factor (ligand) superfamily, member 10 0.170789
AKT1 v-akt murine thymoma viral oncogene homolog 1 0.158605