Oral Ulcer Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A stomatitis characterized by the repeated formation of benign and non-contagious mouth ulcers. (Human Disease Ontology, DOID_9663)
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Genes

19 genes associated with the Oral Ulcer phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
BANK1 B-cell scaffold protein with ankyrin repeats 1
BLK BLK proto-oncogene, Src family tyrosine kinase
CFB complement factor B
CTLA4 cytotoxic T-lymphocyte-associated protein 4
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32)
IL10 interleukin 10
IL21 interleukin 21
IRAK1 interleukin-1 receptor-associated kinase 1
ITGAM integrin, alpha M (complement component 3 receptor 3 subunit)
MBL2 mannose-binding lectin (protein C) 2, soluble
MECP2 methyl CpG binding protein 2
MSH5 mutS homolog 5
PDCD1 programmed cell death 1
PHRF1 PHD and ring finger domains 1
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
PXK PX domain containing serine/threonine kinase
STAT4 signal transducer and activator of transcription 4
TNF tumor necrosis factor
TNFSF4 tumor necrosis factor (ligand) superfamily, member 4