bowen-conradi 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_0050684)
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Genes

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

Symbol Name Standardized Value
EMG1 EMG1 N1-specific pseudouridine methyltransferase 2.60801
RRP8 ribosomal RNA processing 8, methyltransferase, homolog (yeast) 2.30033
RPS18P12 ribosomal protein S18 pseudogene 12 1.63635
RPS18 ribosomal protein S18 1.63635
RNMT RNA (guanine-7-) methyltransferase 1.59072
RPS19 ribosomal protein S19 1.28304
FTSJ2 FtsJ RNA methyltransferase homolog 2 (E. coli) 1.07488
NDUFAB1 NADH dehydrogenase (ubiquinone) 1, alpha/beta subcomplex, 1, 8kDa 1.0383
VWF von Willebrand factor 0.1936