myasthenia gravis Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_437)
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Genes

23 genes associated with the disease myasthenia gravis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ACE angiotensin I converting enzyme
APOE apolipoprotein E
CHRND cholinergic receptor, nicotinic, delta (muscle)
CTLA4 cytotoxic T-lymphocyte-associated protein 4
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32)
FCGR3A Fc fragment of IgG, low affinity IIIa, receptor (CD16a)
FCGR3B Fc fragment of IgG, low affinity IIIb, receptor (CD16b)
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
HLA-C major histocompatibility complex, class I, C
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRA major histocompatibility complex, class II, DR alpha
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IL1A interleukin 1, alpha
IL2RB interleukin 2 receptor, beta
LGALS1 lectin, galactoside-binding, soluble, 1
LTA lymphotoxin alpha
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
TNF tumor necrosis factor