pulmonary vascular congestion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description obstruction of the normal flux of blood within the blood vessel network of the lung resulting in engorgement of pulmonary vessels; frequently precedes pulmonary edema (Mammalian Phenotype Ontology, MP_0010018)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010018
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Genes

22 gene mutations causing the pulmonary vascular congestion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
ABCA3 ATP-binding cassette, sub-family A (ABC1), member 3
ACE2 angiotensin I converting enzyme 2
ADIPOQ adiponectin, C1Q and collagen domain containing
DNM1L dynamin 1-like
EPHA3 EPH receptor A3
GBE1 glucan (1,4-alpha-), branching enzyme 1
GYS1 glycogen synthase 1 (muscle)
HEY2 hes-related family bHLH transcription factor with YRPW motif 2
KIFAP3 kinesin-associated protein 3
LPL lipoprotein lipase
MORF4L1 mortality factor 4 like 1
NOS3 nitric oxide synthase 3 (endothelial cell)
PDLIM7 PDZ and LIM domain 7 (enigma)
PECAM1 platelet/endothelial cell adhesion molecule 1
PIKFYVE phosphoinositide kinase, FYVE finger containing
PNPLA2 patatin-like phospholipase domain containing 2
PTGER4 prostaglandin E receptor 4 (subtype EP4)
RUNX2 runt-related transcription factor 2
SLIT3 slit homolog 3 (Drosophila)
TFAP2B transcription factor AP-2 beta (activating enhancer binding protein 2 beta)
TMEM38B transmembrane protein 38B