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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vascular development
Debug Stats
  • ### Total Build Time: 605 ms 25.646 KB
  • CONCEPT_NAME gt=10 ms Completed: 10 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 4.277 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.938 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=499 ms Completed: 499 ms rowSize= 15.333 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal vascular development MP:0000259
Definition (1)
aberrant process of vascular formation
Synonyms (1)
"vascular development abnormalities" EXACT
Parents (2)
img abnormal blood vessel morphology MP:0001614
img abnormal cardiovascular development MP:0002925
Children (9)
img abnormal vascular smooth muscle development MP:0011401
img abnormal cardinal vein morphology MP:0004783
img abnormal vascular endothelial cell development MP:0003542
img abnormal fetal ductus arteriosus morphology MP:0010564
img abnormal vitelline vasculature morphology MP:0003229
img abnormal vasculogenesis MP:0001622
img abnormal branchial arch artery morphology MP:0002672
img abnormal angiogenesis MP:0000260
img abnormal dorsal aorta morphology MP:0004787
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053855img abnormal blood vessel morphology MP:0001614
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053855img abnormal cardiovascular development MP:0002925
Genes (471)

Species:
human : 471
Page Size
Current 25
  Page 1 of 19
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanECSCR641700endothelial cell surface expressed chemotaxis and apoptosis regulator
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanNRARP441478NOTCH-regulated ankyrin repeat protein
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
INFERRED
HumanUNC5B219699unc-5 homolog B (C. elegans)
INFERRED
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
INFERRED
HumanBMPER168667BMP binding endothelial regulator
INFERRED
HumanZFPM1161882zinc finger protein, FOG family member 1
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
INFERRED
HumanAMOT154796angiomotin
INFERRED
HumanE2F7144455E2F transcription factor 7
INFERRED
HumanCCM2L140706cerebral cavernous malformation 2-like
INFERRED
HumanABRA137735actin-binding Rho activating protein
INFERRED
HumanOSR1130497odd-skipped related 1 (Drosophila)
INFERRED
HumanTWIST2117581twist basic helix-loop-helix transcription factor 2
Click here to display 105 evidence detail records.
HumanNOSTRIN115677nitric oxide synthase trafficking
INFERRED
HumanMYOCD93649myocardin
INFERRED
HumanESAM90952endothelial cell adhesion molecule
INFERRED
HumanSTARD1390627StAR-related lipid transfer (START) domain containing 13
INFERRED
HumanDISP184976dispatched homolog 1 (Drosophila)
Click here to display 105 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000259abnormal vascular development0self