Hypergammaglobulinemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An increased level of gamma globulin (immunoglobulin) in the blood. (Human Phenotype Ontology, HP_0010702)
External Link https://www.disgenet.org/browser/0/1/0/C0020455
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Genes

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

Symbol Name
ACE angiotensin I converting enzyme
ALB albumin
B2M beta-2-microglobulin
BCL2 B-cell CLL/lymphoma 2
BTG3 BTG family, member 3
CALR calreticulin
CD40LG CD40 ligand
CRP C-reactive protein, pentraxin-related
EPO erythropoietin
FAS Fas cell surface death receptor
FCER2 Fc fragment of IgE, low affinity II, receptor for (CD23)
GPT glutamic-pyruvate transaminase (alanine aminotransferase)
IFNA1 interferon, alpha 1
IFNA13 interferon, alpha 13
IFNG interferon, gamma
IFNGR1 interferon gamma receptor 1
IL10 interleukin 10
IL17A interleukin 17A
IL22 interleukin 22
IL33 interleukin 33
IL4 interleukin 4
IL6 interleukin 6
MST1 macrophage stimulating 1
MYD88 myeloid differentiation primary response 88
SLC17A5 solute carrier family 17 (acidic sugar transporter), member 5
SSB Sjogren syndrome antigen B (autoantigen La)
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
STAT5A signal transducer and activator of transcription 5A
STAT5B signal transducer and activator of transcription 5B
TGFB1 transforming growth factor, beta 1
TLR9 toll-like receptor 9
TNF tumor necrosis factor
TRIM21 tripartite motif containing 21
TTC7A tetratricopeptide repeat domain 7A
ZC3H12A zinc finger CCCH-type containing 12A