Granulomatosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Formation of multiple granulomas, i.e., localized nodular foci inflammation. (Human Phenotype Ontology, HP_0002955)
External Link https://www.disgenet.org/browser/0/1/0/C0521173
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Genes

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

Symbol Name
BTNL2 butyrophilin-like 2
CTLA4 cytotoxic T-lymphocyte-associated protein 4
CYBA cytochrome b-245, alpha polypeptide
CYBB cytochrome b-245, beta polypeptide
HLA-DPA1 major histocompatibility complex, class II, DP alpha 1
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
IL17A interleukin 17A
NCF1 neutrophil cytosolic factor 1
NCF2 neutrophil cytosolic factor 2
NOD2 nucleotide-binding oligomerization domain containing 2
PRTN3 proteinase 3
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1
TNF tumor necrosis factor