Berylliosis Gene Set

Dataset CTD Gene-Disease Associations
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D001607
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Genes

11 genes/proteins associated with the disease Berylliosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CD28 CD28 molecule 2.88009
GCLM glutamate-cysteine ligase, modifier subunit 2.88009
HLA-DPB2 major histocompatibility complex, class II, DP beta 2 (pseudogene) 2.88009
HLA-DPB1 major histocompatibility complex, class II, DP beta 1 2.88009
TGFB1 transforming growth factor, beta 1 2.88009
HLA-DRB1 major histocompatibility complex, class II, DR beta 1 2.88009
IL2RA interleukin 2 receptor, alpha 2.88009
ACE angiotensin I converting enzyme 2.88009
TNF tumor necrosis factor 2.88009
BTNL2 butyrophilin-like 2 2.88009
IL6 interleukin 6 2.88009