Erythema Multiforme Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A skin disease that is a type of allergic reaction located_in skin, which occurs in response to medications, infections, or illness. (Human Disease Ontology, DOID_0050185)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D004892
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Genes

21 genes/proteins associated with the disease Erythema Multiforme from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MASP2 mannan-binding lectin serine peptidase 2 2.88009
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.75142
TNF tumor necrosis factor 1.55157
CXCL8 chemokine (C-X-C motif) ligand 8 1.53989
CAT catalase 1.26298
IL4 interleukin 4 1.23712
BCL2 B-cell CLL/lymphoma 2 1.21173
IL1B interleukin 1, beta 1.19312
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 1.17926
COL1A2 collagen, type I, alpha 2 1.16434
ABCC2 ATP-binding cassette, sub-family C (CFTR/MRP), member 2 1.15256
TGFB1 transforming growth factor, beta 1 1.14336
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor) 1.13075
ABCC3 ATP-binding cassette, sub-family C (CFTR/MRP), member 3 1.11843
HMGB1 high mobility group box 1 1.08655
CASP9 caspase 9, apoptosis-related cysteine peptidase 1.07518
NFKB1 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 1.06734
CCL2 chemokine (C-C motif) ligand 2 1.06044
IL10 interleukin 10 1.04831
MAPK1 mitogen-activated protein kinase 1 1.04314
IL6 interleukin 6 1.04014