Vitiligo Gene Set

Dataset	CTD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A disorder consisting of areas of macular depigmentation, commonly on extensor aspects of extremities, on the face or neck, and in skin folds. Age of onset is often in young adulthood and the condition tends to progress gradually with lesions enlarging and extending until a quiescent state is reached. (Experimental Factor Ontology, EFO_0004208)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D014820
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Genes

13 genes/proteins associated with the disease Vitiligo from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
SLA	Src-like-adaptor	2.88009
MC1R	melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)	2.88009
CD44	CD44 molecule (Indian blood group)	2.88009
CCR6	chemokine (C-C motif) receptor 6	2.88009
CASP7	caspase 7, apoptosis-related cysteine peptidase	2.88009
BACH2	BTB and CNC homology 1, basic leucine zipper transcription factor 2	2.88009
IKZF4	IKAROS family zinc finger 4 (Eos)	2.88009
CLNK	cytokine-dependent hematopoietic cell linker	2.88009
CD80	CD80 molecule	2.88009
IFIH1	interferon induced with helicase C domain 1	2.88009
FOXP1	forkhead box P1	2.88009
TOB2	transducer of ERBB2, 2	2.88009
SH2B3	SH2B adaptor protein 3	2.88009