abnormal cardinal vein morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of any of the four veins in the developing vertebrate embryo which run along each side of the vertebral column (Mammalian Phenotype Ontology, MP_0004783)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004783
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Genes

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

Symbol Name
ACVRL1 activin A receptor type II-like 1
BRAF B-Raf proto-oncogene, serine/threonine kinase
CCM2 cerebral cavernous malformation 2
CXADR coxsackie virus and adenovirus receptor
DLL4 delta-like 4 (Drosophila)
EFNB2 ephrin-B2
EPHB4 EPH receptor B4
FLT4 fms-related tyrosine kinase 4
FURIN furin (paired basic amino acid cleaving enzyme)
GLI3 GLI family zinc finger 3
HDAC7 histone deacetylase 7
HSPG2 heparan sulfate proteoglycan 2
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
MYO18B myosin XVIIIB
NR2F2 nuclear receptor subfamily 2, group F, member 2
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PIP5K1C phosphatidylinositol-4-phosphate 5-kinase, type I, gamma
PTPRB protein tyrosine phosphatase, receptor type, B
RBPJ recombination signal binding protein for immunoglobulin kappa J region
TBX18 T-box 18
TLL1 tolloid-like 1
WASF2 WAS protein family, member 2
WNK1 WNK lysine deficient protein kinase 1