abnormal vein development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the process of forming the blood vessels that carry blood to the heart (Mammalian Phenotype Ontology, MP_0003411)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003411
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Genes

27 gene mutations causing the abnormal vein development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVRL1 activin A receptor type II-like 1
ADM adrenomedullin
BRAF B-Raf proto-oncogene, serine/threonine kinase
CCM2 cerebral cavernous malformation 2
CDH5 cadherin 5, type 2 (vascular endothelium)
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
PAM peptidylglycine alpha-amidating monooxygenase
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