abnormal lymph circulation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormalities in the flow of the lymph from the tissues into the veins of the circulatory system (Mammalian Phenotype Ontology, MP_0003659)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003659
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11 gene mutations causing the abnormal lymph circulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EFNB2 ephrin-B2
FLT4 fms-related tyrosine kinase 4
FOXC2 forkhead box C2
HEG1 heart development protein with EGF-like domains 1
ITGA9 integrin, alpha 9
LYVE1 lymphatic vessel endothelial hyaluronan receptor 1
PDPN podoplanin
PPP1R13B protein phosphatase 1, regulatory subunit 13B
PROX1 prospero homeobox 1
TIE1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1
VEGFC vascular endothelial growth factor C