Leprosy Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A chronic granulomatous infection caused by MYCOBACTERIUM LEPRAE. The granulomatous lesions are manifested in the skin, the mucous membranes, and the peripheral nerves. Two polar or principal types are lepromatous and tuberculoid. (Experimental Factor Ontology, EFO_0001054)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D007918
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Genes

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

Symbol Name Standardized Value
PACRG PARK2 co-regulated 2.88009
RAB32 RAB32, member RAS oncogene family 2.88009
LTA lymphotoxin alpha 2.88009
TLR1 toll-like receptor 1 2.88009
TLR2 toll-like receptor 2 2.88009
PARK2 parkin RBR E3 ubiquitin protein ligase 2.88009
LPRS Leprosy, susceptibility to 1 2.88009
LPRS6 Leprosy, susceptiblity to, 6 2.88009
IL23R interleukin 23 receptor 2.88009
CCDC88B coiled-coil domain containing 88B 2.88009
SLC11A1 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 1 2.88009
BATF3 basic leucine zipper transcription factor, ATF-like 3 2.88009