pearson syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A mitochondrial metabolism disease that is characterized by sideroblastic anemia and exocrine pancreas dysfunction. (Human Disease Ontology, DOID_0060067)
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Genes

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

Symbol Name Standardized Value
SLC25A38 solute carrier family 25, member 38 1.55158
GFM1 G elongation factor, mitochondrial 1 1.45177
NPTX2 neuronal pentraxin II 1.40701
TRMU tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase 1.40483
PUS1 pseudouridylate synthase 1 1.34243
GLRX5 glutaredoxin 5 1.33283
ALAS2 5'-aminolevulinate synthase 2 1.25558
SUCLG1 succinate-CoA ligase, alpha subunit 1.20137
ABCB7 ATP-binding cassette, sub-family B (MDR/TAP), member 7 1.15581
POLG polymerase (DNA directed), gamma 1.01047
DGUOK deoxyguanosine kinase 1.00077
DLD dihydrolipoamide dehydrogenase 0.999503
SLC19A2 solute carrier family 19 (thiamine transporter), member 2 0.934556
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like 0.776568
MPV17 MpV17 mitochondrial inner membrane protein 0.773296
OGDH oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) 0.754527
ACO2 aconitase 2, mitochondrial 0.691495
C10ORF2 chromosome 10 open reading frame 2 0.662784
ARSH arylsulfatase family, member H 0.644586
PYGB phosphorylase, glycogen; brain 0.482084
PYGL phosphorylase, glycogen, liver 0.478668
PYGM phosphorylase, glycogen, muscle 0.452585
DNAH8 dynein, axonemal, heavy chain 8 0.424014
HFE hemochromatosis 0.30631