visceral 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 internal organs enclosed within the cavity of the body, such as the thoracic, abdominal, endocrine, and pelvic organs (Mammalian Phenotype Ontology, MP_0010017)
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33 gene mutations causing the visceral 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
ABCA5 ATP-binding cassette, sub-family A (ABC1), member 5
ACE2 angiotensin I converting enzyme 2
ADIPOQ adiponectin, C1Q and collagen domain containing
CXCR4 chemokine (C-X-C motif) receptor 4
DNM1L dynamin 1-like
EPAS1 endothelial PAS domain protein 1
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
LDB3 LIM domain binding 3
LIF leukemia inhibitory factor
LPL lipoprotein lipase
MORF4L1 mortality factor 4 like 1
NOS3 nitric oxide synthase 3 (endothelial cell)
NOV nephroblastoma overexpressed
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)
PTGIS prostaglandin I2 (prostacyclin) synthase
RUNX2 runt-related transcription factor 2
SHC1 SHC (Src homology 2 domain containing) transforming protein 1
SLC14A2 solute carrier family 14 (urea transporter), member 2
SLIT3 slit homolog 3 (Drosophila)
SPTA1 spectrin, alpha, erythrocytic 1
TFAP2B transcription factor AP-2 beta (activating enhancer binding protein 2 beta)
TH tyrosine hydroxylase
TMEM38B transmembrane protein 38B