Alopecia Areata Gene Set

Dataset	CTD 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)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D000506
Similar Terms
Downloads & Tools

Genes

10 genes/proteins associated with the disease Alopecia Areata from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
CXCR3	chemokine (C-X-C motif) receptor 3	2.88009
STX17	syntaxin 17	2.88009
ULBP3	UL16 binding protein 3	2.88009
RAET1L	retinoic acid early transcript 1L	2.88009
CXCL9	chemokine (C-X-C motif) ligand 9	2.88009
IL2RA	interleukin 2 receptor, alpha	2.88009
IKZF4	IKAROS family zinc finger 4 (Eos)	2.88009
PRDX5	peroxiredoxin 5	2.88009
CTLA4	cytotoxic T-lymphocyte-associated protein 4	2.88009
CXCL10	chemokine (C-X-C motif) ligand 10	2.88009