vascular smooth muscle cell hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased numbers of smooth muscle cells in the vascular wall (Mammalian Phenotype Ontology, MP_0005489)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005489
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Genes

10 gene mutations causing the vascular smooth muscle cell hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
ARNTL aryl hydrocarbon receptor nuclear translocator-like
EFEMP2 EGF containing fibulin-like extracellular matrix protein 2
ITGA7 integrin, alpha 7
PGR progesterone receptor
PRKCD protein kinase C, delta
REN renin
SERPIND1 serpin peptidase inhibitor, clade D (heparin cofactor), member 1
THBS1 thrombospondin 1
VAV2 vav 2 guanine nucleotide exchange factor