abnormal vascular endothelial cell development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the differentiation of the cells that line the vasculature (Mammalian Phenotype Ontology, MP_0003542)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003542
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25 gene mutations causing the abnormal vascular endothelial cell development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARHGEF4 Rho guanine nucleotide exchange factor (GEF) 4
CCM2 cerebral cavernous malformation 2
CDH5 cadherin 5, type 2 (vascular endothelium)
CREBBP CREB binding protein
DOCK1 dedicator of cytokinesis 1
ECSCR endothelial cell surface expressed chemotaxis and apoptosis regulator
FGF2 fibroblast growth factor 2 (basic)
GBX2 gastrulation brain homeobox 2
HPRT1 hypoxanthine phosphoribosyltransferase 1
MAP2K1 mitogen-activated protein kinase kinase 1
MAPK7 mitogen-activated protein kinase 7
MED1 mediator complex subunit 1
MEF2C myocyte enhancer factor 2C
OTULIN OTU deubiquitinase with linear linkage specificity
PLCG1 phospholipase C, gamma 1
PLXND1 plexin D1
POFUT2 protein O-fucosyltransferase 2
PTK2 protein tyrosine kinase 2
PTK2B protein tyrosine kinase 2 beta
RASA3 RAS p21 protein activator 3
RASIP1 Ras interacting protein 1
TGFB1 transforming growth factor, beta 1
TIE1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1
VEGFA vascular endothelial growth factor A
WASF2 WAS protein family, member 2