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Details
Link-It Detail - Jax Mouse Phenotype - persistence of hyaloid vascular system
Debug Stats
  • ### Total Build Time: 36 ms 17.115 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 404 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 338 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 197 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.907 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=27 ms Completed: 27 ms rowSize= 10.938 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.176 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
persistence of hyaloid vascular system MP:0001289
Definition (1)
failure of the degeneration of the transient vascular system of the eye during development, that normally nourishes the retina, immature lens and primary vitreous of the developing eye
Synonyms (1)
"persistence of hyaloid capillary system" EXACT
Parents (2)
img abnormal eye development MP:0001286
img abnormal vitreous body morphology MP:0002699
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053915img abnormal eye development MP:0001286
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053916img abnormal vitreous body morphology MP:0002699
Genes (18)

Species:
human : 18
SpeciesGeneGeneIdGene NameEvidence
HumanLAMA1284217laminin, alpha 1
Click here to display 33 evidence detail records.
HumanCOL18A180781collagen, type XVIII, alpha 1
Click here to display 33 evidence detail records.
HumanLEF151176lymphoid enhancer-binding factor 1
Click here to display 33 evidence detail records.
HumanTSPAN1223554tetraspanin 12
Click here to display 33 evidence detail records.
HumanGNPAT8443glyceronephosphate O-acyltransferase
Click here to display 33 evidence detail records.
HumanFZD48322frizzled family receptor 4
Click here to display 33 evidence detail records.
HumanWNT7B7477wingless-type MMTV integration site family, member 7B
Click here to display 33 evidence detail records.
HumanVEGFA7422vascular endothelial growth factor A
Click here to display 33 evidence detail records.
HumanNR2E17101nuclear receptor subfamily 2, group E, member 1
Click here to display 33 evidence detail records.
HumanTGFB27042transforming growth factor, beta 2
Click here to display 33 evidence detail records.
HumanRPL246152ribosomal protein L24
Click here to display 33 evidence detail records.
HumanRARB5915retinoic acid receptor, beta
Click here to display 33 evidence detail records.
HumanPTPRF5792protein tyrosine phosphatase, receptor type, F
Click here to display 33 evidence detail records.
HumanLRP54041low density lipoprotein receptor-related protein 5
Click here to display 33 evidence detail records.
HumanBMP4652bone morphogenetic protein 4
Click here to display 33 evidence detail records.
HumanAPAF1317apoptotic peptidase activating factor 1
Click here to display 33 evidence detail records.
HumanANGPT2285angiopoietin 2
Click here to display 33 evidence detail records.
HumanAHR196aryl hydrocarbon receptor
Click here to display 33 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001289persistence of hyaloid vascular system0self