increased cerebral infarction size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased size of necrotic area of the cerebrum resulting from a sudden insufficiency of arterial or venous blood supply (Mammalian Phenotype Ontology, MP_0006060)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006060
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Genes

22 gene mutations causing the increased cerebral infarction size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CAMK2A calcium/calmodulin-dependent protein kinase II alpha
CAV1 caveolin 1, caveolae protein, 22kDa
CNR1 cannabinoid receptor 1 (brain)
CNTF ciliary neurotrophic factor
CST3 cystatin C
ENTPD1 ectonucleoside triphosphate diphosphohydrolase 1
F2RL1 coagulation factor II (thrombin) receptor-like 1
FAIM2 Fas apoptotic inhibitory molecule 2
GPX1 glutathione peroxidase 1
GSN gelsolin
HSPA1B heat shock 70kDa protein 1B
IL10 interleukin 10
ITPRIP inositol 1,4,5-trisphosphate receptor interacting protein
NDRG4 NDRG family member 4
NEIL3 nei endonuclease VIII-like 3 (E. coli)
NFE2L2 nuclear factor, erythroid 2-like 2
NOTCH3 notch 3
PSPN persephin
PTGER2 prostaglandin E receptor 2 (subtype EP2), 53kDa
SLC8A3 solute carrier family 8 (sodium/calcium exchanger), member 3
STIP1 stress-induced phosphoprotein 1