Chronic Berylliosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0221052
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Genes

25 genes associated with the disease Chronic Berylliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BTNL2 butyrophilin-like 2
CCR5 chemokine (C-C motif) receptor 5 (gene/pseudogene)
CEL carboxyl ester lipase
CTLA4 cytotoxic T-lymphocyte-associated protein 4
FCGR3A Fc fragment of IgG, low affinity IIIa, receptor (CD16a)
FCGR3B Fc fragment of IgG, low affinity IIIb, receptor (CD16b)
FGF2 fibroblast growth factor 2 (basic)
FOLH1 folate hydrolase (prostate-specific membrane antigen) 1
GSTT1 glutathione S-transferase theta 1
HLA-DPA1 major histocompatibility complex, class II, DP alpha 1
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HLA-DRB3 major histocompatibility complex, class II, DR beta 3
IL1A interleukin 1, alpha
IL9 interleukin 9
IL9R interleukin 9 receptor
ITGAL integrin, alpha L (antigen CD11A (p180), lymphocyte function-associated antigen 1; alpha polypeptide)
ITGB2 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit)
NAT2 N-acetyltransferase 2 (arylamine N-acetyltransferase)
PARP9 poly (ADP-ribose) polymerase family, member 9
PMP22 peripheral myelin protein 22
SLC27A5 solute carrier family 27 (fatty acid transporter), member 5
TGFB1 transforming growth factor, beta 1
TNF tumor necrosis factor
UCHL1 ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)