intracerebral hemorrhage Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Hemorrhage into the parenchyma of the brain. (Human Phenotype Ontology, HP_0001342)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001916
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Genes

33 gene mutations causing the intracerebral hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRA2 adhesion G protein-coupled receptor A2
ANXA7 annexin A7
APAF1 apoptotic peptidase activating factor 1
BIRC6 baculoviral IAP repeat containing 6
BRAF B-Raf proto-oncogene, serine/threonine kinase
CASP9 caspase 9, apoptosis-related cysteine peptidase
CBFB core-binding factor, beta subunit
COL4A1 collagen, type IV, alpha 1
CYCS cytochrome c, somatic
E2F5 E2F transcription factor 5, p130-binding
F3 coagulation factor III (thromboplastin, tissue factor)
FBLN1 fibulin 1
FLI1 Fli-1 proto-oncogene, ETS transcription factor
HSF2 heat shock transcription factor 2
ITGAV integrin, alpha V
ITGB8 integrin, beta 8
JAM3 junctional adhesion molecule 3
KIF27 kinesin family member 27
LLGL1 lethal giant larvae homolog 1 (Drosophila)
MAPK7 mitogen-activated protein kinase 7
MSI1 musashi RNA-binding protein 1
NME5 NME/NM23 family member 5
PLAT plasminogen activator, tissue
PSEN1 presenilin 1
RHBDF1 rhomboid 5 homolog 1 (Drosophila)
RUNX1 runt-related transcription factor 1
SYK spleen tyrosine kinase
TP73 tumor protein p73
UBE4B ubiquitination factor E4B
ULK4 unc-51 like kinase 4
USP18 ubiquitin specific peptidase 18
VKORC1 vitamin K epoxide reductase complex, subunit 1
YBX1 Y box binding protein 1