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Details
Link-It Detail - Jax Mouse Phenotype - abnormal capillary morphology
Debug Stats
  • ### Total Build Time: 190 ms 21.277 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 424 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 178 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= 587 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 593 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.585 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=170 ms Completed: 170 ms rowSize= 16.264 KB
  • CONCEPT_XREFS gt=8 ms Completed: 8 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 capillary morphology MP:0003658
Definition (1)
any structural anomaly of the small branching blood vessels that form a network between the arterioles and venules, where the exchange of water, oxygen, carbon dioxide, and other nutrient and waste chemical substances occurs between the blood and the surrounding tissues
Synonyms (1)
"abnormal capillaries" EXACT
Parents (1)
img abnormal blood vessel morphology MP:0001614
Children (1)
img abnormal kidney capillary morphology MP:0011310
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053855img abnormal blood vessel morphology MP:0001614
Genes (81)

Species:
human : 81
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SpeciesGeneGeneIdGene NameEvidence
HumanUNC5B219699unc-5 homolog B (C. elegans)
Click here to display 61 evidence detail records.
HumanAMOT154796angiomotin
Click here to display 61 evidence detail records.
HumanPLVAP83483plasmalemma vesicle associated protein
Click here to display 61 evidence detail records.
HumanFRAS180144Fraser syndrome 1
INFERRED
HumanZMIZ157178zinc finger, MIZ-type containing 1
Click here to display 61 evidence detail records.
HumanC1GALT156913core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1
Click here to display 61 evidence detail records.
HumanDLL454567delta-like 4 (Drosophila)
Click here to display 61 evidence detail records.
HumanHSD17B751478hydroxysteroid (17-beta) dehydrogenase 7
Click here to display 61 evidence detail records.
HumanGOLM151280golgi membrane protein 1
INFERRED
HumanCRIM151232cysteine rich transmembrane BMP regulator 1 (chordin-like)
INFERRED
HumanANGPTL451129angiopoietin-like 4
Click here to display 61 evidence detail records.
HumanRRM2B50484ribonucleotide reductase M2 B (TP53 inducible)
INFERRED
HumanEHD430844EH-domain containing 4
INFERRED
HumanANKRD1726057ankyrin repeat domain 17
Click here to display 61 evidence detail records.
HumanSNX1323161sorting nexin 13
Click here to display 61 evidence detail records.
HumanTUSC211334tumor suppressor candidate 2
INFERRED
HumanPROKR110887prokineticin receptor 1
Click here to display 61 evidence detail records.
HumanTRAF3IP210758TRAF3 interacting protein 2
INFERRED
HumanTAB110454TGF-beta activated kinase 1/MAP3K7 binding protein 1
Click here to display 61 evidence detail records.
HumanWASF210163WAS protein family, member 2
Click here to display 61 evidence detail records.
HumanEBI310148Epstein-Barr virus induced 3
INFERRED
HumanBCL2L1110018BCL2-like 11 (apoptosis facilitator)
INFERRED
HumanAPLN8862apelin
Click here to display 61 evidence detail records.
HumanNPHS27827nephrosis 2, idiopathic, steroid-resistant (podocin)
INFERRED
HumanVEZF17716vascular endothelial zinc finger 1
Click here to display 61 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003658abnormal capillary morphology0self