abnormal anterior cardinal vein morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the two paired veins draining the cephalic part of the body (Mammalian Phenotype Ontology, MP_0004784)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004784
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Genes

11 gene mutations causing the abnormal anterior cardinal vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVRL1 activin A receptor type II-like 1
DLL4 delta-like 4 (Drosophila)
EFNB2 ephrin-B2
EPHB4 EPH receptor B4
FLT4 fms-related tyrosine kinase 4
GLI3 GLI family zinc finger 3
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NR2F2 nuclear receptor subfamily 2, group F, member 2
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
RBPJ recombination signal binding protein for immunoglobulin kappa J region
WASF2 WAS protein family, member 2