brain infarction Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

18 genes associated with the disease brain infarction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TWIST1 twist family bHLH transcription factor 1 1.14929
HDAC9 histone deacetylase 9 0.790827
NINJ2 ninjurin 2 0.63207
ZFHX3 zinc finger homeobox 3 0.486425
ASB3 ankyrin repeat and SOCS box containing 3 0.438544
SUPT3H suppressor of Ty 3 homolog (S. cerevisiae) 0.438544
PRKCH protein kinase C, eta 0.311576
SPSB4 splA/ryanodine receptor domain and SOCS box containing 4 0.297866
IMPA2 inositol(myo)-1(or 4)-monophosphatase 2 0.285417
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial) 0.256228
FRY furry homolog (Drosophila) 0.197766
DLG2 discs, large homolog 2 (Drosophila) 0.15771
PCGF5 polycomb group ring finger 5 0.080593
MEOX2 mesenchyme homeobox 2 0.080593
ADCY8 adenylate cyclase 8 (brain) 0.064973
RPL14P1 ribosomal protein L14 pseudogene 1 0.043246
AIM1 absent in melanoma 1 0.043246
KIAA0020 KIAA0020 0.043246