heart inflammation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description local accumulation of fluid, plasma proteins, and leukocytes in the heart (Mammalian Phenotype Ontology, MP_0001853)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001853
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28 gene mutations causing the heart inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AHR aryl hydrocarbon receptor
APEX1 APEX nuclease (multifunctional DNA repair enzyme) 1
ARIH2 ariadne RBR E3 ubiquitin protein ligase 2
BCL6 B-cell CLL/lymphoma 6
CHD2 chromodomain helicase DNA binding protein 2
CLU clusterin
CTLA4 cytotoxic T-lymphocyte-associated protein 4
DMD dystrophin
GJA1 gap junction protein, alpha 1, 43kDa
IL2 interleukin 2
MAP3K1 mitogen-activated protein kinase kinase kinase 1, E3 ubiquitin protein ligase
MMP9 matrix metallopeptidase 9
NCKAP1L NCK-associated protein 1-like
PPARA peroxisome proliferator-activated receptor alpha
PPIA peptidylprolyl isomerase A (cyclophilin A)
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SGCA sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)
SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4
SOCS1 suppressor of cytokine signaling 1
TAX1BP1 Tax1 (human T-cell leukemia virus type I) binding protein 1
TGFB1 transforming growth factor, beta 1
TICAM1 toll-like receptor adaptor molecule 1
TLR3 toll-like receptor 3
TREX1 three prime repair exonuclease 1
WRN Werner syndrome, RecQ helicase-like
XCL1 chemokine (C motif) ligand 1
ZFP36 ZFP36 ring finger protein