dilated vasculature Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description stretched or widened aperture of the luminal space of the network of tubes that carries blood through the body (Mammalian Phenotype Ontology, MP_0004938)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004938
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19 gene mutations causing the dilated vasculature phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVRL1 activin A receptor type II-like 1
AMOT angiomotin
ANTXR2 anthrax toxin receptor 2
CDSN corneodesmosin
CYP2E1 cytochrome P450, family 2, subfamily E, polypeptide 1
G6PD glucose-6-phosphate dehydrogenase
KRIT1 KRIT1, ankyrin repeat containing
MLST8 MTOR associated protein, LST8 homolog (S. cerevisiae)
NCOA6 nuclear receptor coactivator 6
PARVA parvin, alpha
PDLIM7 PDZ and LIM domain 7 (enigma)
PNPLA6 patatin-like phospholipase domain containing 6
RECK reversion-inducing-cysteine-rich protein with kazal motifs
RUNX1 runt-related transcription factor 1
SYK spleen tyrosine kinase
TCF7L1 transcription factor 7-like 1 (T-cell specific, HMG-box)
TIE1 tyrosine kinase with immunoglobulin-like and EGF-like domains 1
TSC2 tuberous sclerosis 2
VCL vinculin