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8 genes annotated in human

cerebrovascular disease

DOID:6713

An artery disease that is characterized by dysfunction of the blood vessels supplying the brain.

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Known genes in the process in human Include functional analogs

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Show only novel predictions Show only unknown genes Highlight genes with functional analogs involved in "cerebrovascular disease" (in gray)

Name	Description	Probability	Func Analog Organism
NOSTRIN	nitric oxide synthase trafficker	0.956
GUCY1B3	guanylate cyclase 1, soluble, beta 3	0.899	Human
PARP9	poly (ADP-ribose) polymerase family, member 9	0.098
FGA	fibrinogen alpha chain	0.037
MYH11	myosin, heavy chain 11, smooth muscle	0.030
ALOX5	arachidonate 5-lipoxygenase	0.023
C5orf56	chromosome 5 open reading frame 56	0.020
NLRC5	NLR family, CARD domain containing 5	0.017
ALB	albumin	0.016
DTX3L	deltex 3-like (Drosophila)	0.016
LAPTM5	lysosomal protein transmembrane 5	0.012
LCP1	lymphocyte cytosolic protein 1 (L-plastin)	0.011
CDC37	cell division cycle 37 homolog (S. cerevisiae)	0.011
F5	coagulation factor V (proaccelerin, labile factor)	0.003
NOS3	nitric oxide synthase 3 (endothelial cell)	0.002
PRKCH	protein kinase C, eta	0.002
GUCY1A3	guanylate cyclase 1, soluble, alpha 3	0.002
ACTA2	actin, alpha 2, smooth muscle, aorta	0.002
F2	coagulation factor II (thrombin)	0.001
ALOX5AP	arachidonate 5-lipoxygenase-activating protein	0.001
RNF213	ring finger protein 213	0.000