insulitis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a histological change in the islets of Langerhans characterized by edema and the infiltration of small numbers of white blood cells (Mammalian Phenotype Ontology, MP_0004031)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004031
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Genes

22 gene mutations causing the insulitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AIRE autoimmune regulator
B2M beta-2-microglobulin
CD38 CD38 molecule
CIITA class II, major histocompatibility complex, transactivator
CTSB cathepsin B
CTSS cathepsin S
CTSV cathepsin V
E2F1 E2F transcription factor 1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
ICOS inducible T-cell co-stimulator
IGHM immunoglobulin heavy constant mu
IL4 interleukin 4
INS insulin
MERTK MER proto-oncogene, tyrosine kinase
MTUS1 microtubule associated tumor suppressor 1
PDCD1LG2 programmed cell death 1 ligand 2
PLA2G4A phospholipase A2, group IVA (cytosolic, calcium-dependent)
PRF1 perforin 1 (pore forming protein)
PTPRN protein tyrosine phosphatase, receptor type, N
RAPGEF3 Rap guanine nucleotide exchange factor (GEF) 3
TLR2 toll-like receptor 2
TNFRSF9 tumor necrosis factor receptor superfamily, member 9