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Details
Link-It Detail - Jax Mouse Phenotype - abnormal brain vasculature morphology
Debug Stats
  • ### Total Build Time: 272 ms 24.314 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 402 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 217 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 1.024 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.471 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.922 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=266 ms Completed: 266 ms rowSize= 16.974 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal brain vasculature morphology MP:0004950
Definition (1)
any structural anomaly of the blood vessel network of the brain
Parents (2)
img abnormal blood vessel morphology MP:0001614
img abnormal brain morphology MP:0002152
Children (3)
img brain aneurysm MP:0010479
img cerebral arteriovenous malformation MP:0010530
img brain vascular congestion MP:0010022
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 nervous system phenotype MP:00036315img abnormal brain morphology MP:0002152
Genes (41)

Species:
human : 41
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SpeciesGeneGeneIdGene NameEvidence
HumanAMOT154796angiomotin
Click here to display 76 evidence detail records.
HumanCCM283605cerebral cavernous malformation 2
Click here to display 76 evidence detail records.
HumanWNK165125WNK lysine deficient protein kinase 1
Click here to display 76 evidence detail records.
HumanARAP364411ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3
Click here to display 76 evidence detail records.
HumanMKL257496MKL/myocardin-like 2
Click here to display 76 evidence detail records.
HumanFBXW755294F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase
Click here to display 76 evidence detail records.
HumanCC2D1A54862coiled-coil and C2 domain containing 1A
Click here to display 76 evidence detail records.
HumanSUFU51684suppressor of fused homolog (Drosophila)
INFERRED
HumanCLEC1B51266C-type lectin domain family 1, member B
Click here to display 76 evidence detail records.
HumanEPN129924epsin 1
Click here to display 76 evidence detail records.
HumanTNFRSF2127242tumor necrosis factor receptor superfamily, member 21
Click here to display 76 evidence detail records.
HumanGPR12425960G protein-coupled receptor 124
Click here to display 76 evidence detail records.
HumanPDCD1011235programmed cell death 10
Click here to display 76 evidence detail records.
HumanNR1H310062nuclear receptor subfamily 1, group H, member 3
Click here to display 76 evidence detail records.
HumanNRP18829neuropilin 1
Click here to display 76 evidence detail records.
HumanRECK8434reversion-inducing-cysteine-rich protein with kazal motifs
Click here to display 76 evidence detail records.
HumanFZD48322frizzled family receptor 4
Click here to display 76 evidence detail records.
HumanVEGFA7422vascular endothelial growth factor A
Click here to display 76 evidence detail records.
HumanTGFB17040transforming growth factor, beta 1
Click here to display 76 evidence detail records.
HumanADAM176868ADAM metallopeptidase domain 17
Click here to display 76 evidence detail records.
HumanSYK6850spleen tyrosine kinase
Click here to display 76 evidence detail records.
HumanPTEN5728phosphatase and tensin homolog
Click here to display 76 evidence detail records.
HumanPSEN15663presenilin 1
Click here to display 76 evidence detail records.
HumanPROS15627protein S (alpha)
Click here to display 76 evidence detail records.
HumanPKD15310polycystic kidney disease 1 (autosomal dominant)
Click here to display 76 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004950abnormal brain vasculature morphology0self