abnormal blood flow velocity Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the rate of flow of the blood through vessels (Mammalian Phenotype Ontology, MP_0000233)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000233
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29 gene mutations causing the abnormal blood flow velocity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACTA2 actin, alpha 2, smooth muscle, aorta
ADORA3 adenosine A3 receptor
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR2 angiotensin II receptor, type 2
APOE apolipoprotein E
CITED2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
COL2A1 collagen, type II, alpha 1
CYBB cytochrome b-245, beta polypeptide
DCBLD2 discoidin, CUB and LCCL domain containing 2
ENTPD1 ectonucleoside triphosphate diphosphohydrolase 1
ERBB4 erb-b2 receptor tyrosine kinase 4
KLF3 Kruppel-like factor 3 (basic)
LOX lysyl oxidase
MAS1 MAS1 proto-oncogene, G protein-coupled receptor
MB myoglobin
MUS81 MUS81 structure-specific endonuclease subunit
NOS1 nitric oxide synthase 1 (neuronal)
NOS3 nitric oxide synthase 3 (endothelial cell)
NPAS2 neuronal PAS domain protein 2
NT5E 5'-nucleotidase, ecto (CD73)
PTGER3 prostaglandin E receptor 3 (subtype EP3)
PTGS1 prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
RGS4 regulator of G-protein signaling 4
SLC14A2 solute carrier family 14 (urea transporter), member 2
SPP1 secreted phosphoprotein 1
TIMP4 TIMP metallopeptidase inhibitor 4
TNS1 tensin 1
TRPV1 transient receptor potential cation channel, subfamily V, member 1
TXNRD2 thioredoxin reductase 2