berylliosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A pneumoconiosis that involves allergic response located_in lungs caused by inhalation of beryllium compounds. (Human Disease Ontology, DOID_10322)
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Genes

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

Symbol Name Standardized Value
HLA-DPB1 major histocompatibility complex, class II, DP beta 1 1.45265
HLA-DPA1 major histocompatibility complex, class II, DP alpha 1 0.828229
TFDP3 transcription factor Dp family, member 3 0.819616
HLA-DMA major histocompatibility complex, class II, DM alpha 0.6939
POMC proopiomelanocortin 0.608494
HGS hepatocyte growth factor-regulated tyrosine kinase substrate 0.590948
CTSA cathepsin A 0.499614
HLA-C major histocompatibility complex, class I, C 0.43227
ACE angiotensin I converting enzyme 0.416521
HLA-DRB1 major histocompatibility complex, class II, DR beta 1 0.416147
ALPPL2 alkaline phosphatase, placental-like 2 0.396353
ALPP alkaline phosphatase, placental 0.39598
ALPL alkaline phosphatase, liver/bone/kidney 0.395235
HLA-DRB4 major histocompatibility complex, class II, DR beta 4 0.389281
HLA-DRB5 major histocompatibility complex, class II, DR beta 5 0.369628
IL2 interleukin 2 0.358183
HLA-DQB3 major histocompatibility complex, class II, DQ beta 3 0.301976
CD4 CD4 molecule 0.298371
CTSK cathepsin K 0.293694
ACPP acid phosphatase, prostate 0.278297