increased vasodilation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than the expected or normal widening of the lumen of the blood vessels (Mammalian Phenotype Ontology, MP_0005590)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005590
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Genes

17 gene mutations causing the increased vasodilation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVRL1 activin A receptor type II-like 1
AGXT2 alanine--glyoxylate aminotransferase 2
BCAR1 breast cancer anti-estrogen resistance 1
CAV1 caveolin 1, caveolae protein, 22kDa
CCL13 chemokine (C-C motif) ligand 13
CHRD chordin
CRK v-crk avian sarcoma virus CT10 oncogene homolog
ESR2 estrogen receptor 2 (ER beta)
GPSM1 G-protein signaling modulator 1
NOS3 nitric oxide synthase 3 (endothelial cell)
PLOD3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
POMT1 protein-O-mannosyltransferase 1
PSEN1 presenilin 1
PTGDR prostaglandin D2 receptor (DP)
PTGER3 prostaglandin E receptor 3 (subtype EP3)
SHC1 SHC (Src homology 2 domain containing) transforming protein 1
SMTNL1 smoothelin-like 1