increased cellular sensitivity to hydrogen peroxide Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater incidence of cell death following exposure to hydrogen peroxide (Mammalian Phenotype Ontology, MP_0008406)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008406
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Genes

21 gene mutations causing the increased cellular sensitivity to hydrogen peroxide phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AIFM1 apoptosis-inducing factor, mitochondrion-associated, 1
ATMIN ATM interactor
CC2D1A coiled-coil and C2 domain containing 1A
CP ceruloplasmin (ferroxidase)
CRYBB2 crystallin, beta B2
GCLM glutamate-cysteine ligase, modifier subunit
GPX1 glutathione peroxidase 1
GPX7 glutathione peroxidase 7
MAPKAP1 mitogen-activated protein kinase associated protein 1
MIR144 microRNA 144
MIR451A microRNA 451a
NFE2L2 nuclear factor, erythroid 2-like 2
PRDX1 peroxiredoxin 1
PRDX2 peroxiredoxin 2
RIT1 Ras-like without CAAX 1
SESN2 sestrin 2
SIRT7 sirtuin 7
SLC1A1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
SLC1A3 solute carrier family 1 (glial high affinity glutamate transporter), member 3
STC2 stanniocalcin 2
VASN vasorin