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Details
Link-It Detail - Jax Mouse Phenotype - abnormal primary vitreous morphology
Debug Stats
  • ### Total Build Time: 18 ms 11.580 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 400 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 330 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
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  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 1.024 KB
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.037 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.907 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 4.580 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.174 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal primary vitreous morphology MP:0009620
Definition (1)
any structural anomaly in the fibrovascular mesodermal tissue located between the optic cup and lens vesicle that normally regresses during the development of the vitreous body
Parents (2)
img abnormal eye development MP:0001286
img abnormal vitreous body morphology MP:0002699
Children (2)
img persistent hyperplastic primary vitreous MP:0010711
img primary vitreous hyperplasia MP:0009621
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 (9)

Species:
human : 9
SpeciesGeneGeneIdGene NameEvidence
HumanSTRA664220stimulated by retinoic acid 6
INFERRED
HumanTGFB27042transforming growth factor, beta 2
INFERRED
HumanRXRA6256retinoid X receptor, alpha
INFERRED
HumanRARB5915retinoic acid receptor, beta
INFERRED
HumanRARA5914retinoic acid receptor, alpha
INFERRED
HumanNOTCH24853notch 2
INFERRED
HumanCDKN2A1029cyclin-dependent kinase inhibitor 2A
INFERRED
HumanALDH1A3220aldehyde dehydrogenase 1 family, member A3
INFERRED
HumanALDH1A1216aldehyde dehydrogenase 1 family, member A1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009620abnormal primary vitreous morphology0self