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Details
Link-It Detail - Jax Mouse Phenotype - absent dentate gyrus
Debug Stats
  • ### Total Build Time: 19 ms 11.939 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 368 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 315 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 182 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 588 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.925 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 6.285 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.158 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
absent dentate gyrus MP:0000814
Definition (1)
lack of the section of the hippocampus normally situated above the gyrus hippocampi and composed of three layers, the molecular, granular, and polymorphic layers
Synonyms (1)
"absence of dentate gyrus" EXACT
Parents (1)
img abnormal dentate gyrus morphology MP:0000812
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img abnormal dentate gyrus morphology MP:0000812
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal dentate gyrus morphology MP:0000812
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanLHX564211LIM homeobox 5
Click here to display 17 evidence detail records.
HumanNEUROD663974neuronal differentiation 6
Click here to display 17 evidence detail records.
HumanFEZF255079FEZ family zinc finger 2
Click here to display 17 evidence detail records.
HumanLEF151176lymphoid enhancer-binding factor 1
Click here to display 17 evidence detail records.
HumanNFIB4781nuclear factor I/B
Click here to display 17 evidence detail records.
HumanNEUROD14760neuronal differentiation 1
Click here to display 17 evidence detail records.
HumanEMX22018empty spiracles homeobox 2
Click here to display 17 evidence detail records.
HumanEMX12016empty spiracles homeobox 1
Click here to display 17 evidence detail records.
HumanCTNNB11499catenin (cadherin-associated protein), beta 1, 88kDa
Click here to display 17 evidence detail records.
HumanATRX546alpha thalassemia/mental retardation syndrome X-linked
Click here to display 17 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000814absent dentate gyrus0self