abnormal endocardium morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the thin serous membrane, primarily composed of endothelial tissue, that lines the interior of the heart (Mammalian Phenotype Ontology, MP_0003974)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003974
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25 gene mutations causing the abnormal endocardium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABI1 abl-interactor 1
ACVRL1 activin A receptor type II-like 1
ADGRG6 adhesion G protein-coupled receptor G6
ANGPT1 angiopoietin 1
EFNB2 ephrin-B2
ENG endoglin
EPHB4 EPH receptor B4
FLRT2 fibronectin leucine rich transmembrane protein 2
FN1 fibronectin 1
HEY2 hes-related family bHLH transcription factor with YRPW motif 2
IDUA iduronidase, alpha-L-
MAPK7 mitogen-activated protein kinase 7
MEF2C myocyte enhancer factor 2C
OVOL2 ovo-like zinc finger 2
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PTK2 protein tyrosine kinase 2
PTPRJ protein tyrosine phosphatase, receptor type, J
RASIP1 Ras interacting protein 1
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SLC8A1 solute carrier family 8 (sodium/calcium exchanger), member 1
SMAD6 SMAD family member 6
THBD thrombomodulin
TIE1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1
TSC2 tuberous sclerosis 2
WASF2 WAS protein family, member 2