abnormal intersomitic vessel morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the primary blood vessel sprouts that originate from the dorsal aorta and posterior cardinal vein and align dorsoventrally at the myotomal boundaries between somites (Mammalian Phenotype Ontology, MP_0012253)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012253
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24 gene mutations causing the abnormal intersomitic vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVRL1 activin A receptor type II-like 1
ADAM10 ADAM metallopeptidase domain 10
CDH5 cadherin 5, type 2 (vascular endothelium)
EFNB2 ephrin-B2
ENG endoglin
FLNA filamin A, alpha
FOXO1 forkhead box O1
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
KRIT1 KRIT1, ankyrin repeat containing
MAPK7 mitogen-activated protein kinase 7
MIB1 mindbomb E3 ubiquitin protein ligase 1
MYL7 myosin, light chain 7, regulatory
NKX2-5 NK2 homeobox 5
OVOL2 ovo-like zinc finger 2
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PLXND1 plexin D1
POFUT1 protein O-fucosyltransferase 1
POGLUT1 protein O-glucosyltransferase 1
PTPRB protein tyrosine phosphatase, receptor type, B
PTPRJ protein tyrosine phosphatase, receptor type, J
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
TBX6 T-box 6
WASF2 WAS protein family, member 2
ZFP36L1 ZFP36 ring finger protein-like 1