alopecia areata Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A hypersensitivity reaction type II disease resulting in the loss of hair on the scalp and elsewhere on the body initially causing bald spots. (Human Disease Ontology, DOID_986)
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Genes

19 genes associated with the disease alopecia areata in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol	Name
C5	complement component 5
FAS	Fas cell surface death receptor
FASLG	Fas ligand (TNF superfamily, member 6)
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-DRB1	major histocompatibility complex, class II, DR beta 1
IL1A	interleukin 1, alpha
IL1B	interleukin 1, beta
IL1RN	interleukin 1 receptor antagonist
IL2RA	interleukin 2 receptor, alpha
MIF	macrophage migration inhibitory factor (glycosylation-inhibiting factor)
NOTCH4	notch 4
PTPN22	protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
STX17	syntaxin 17
TRAF1	TNF receptor-associated factor 1
VDR	vitamin D (1,25- dihydroxyvitamin D3) receptor