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Details
Link-It Detail - Jax Mouse Phenotype - impaired cued conditioning behavior
Debug Stats
  • ### Total Build Time: 126 ms 18.915 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 398 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 404 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 189 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=10 ms Completed: 10 ms rowSize= 590 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 1.588 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=94 ms Completed: 94 ms rowSize= 14.458 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.173 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
impaired cued conditioning behavior MP:0009456
Definition (1)
decrease in the ability of an animal to learn and remember an association between an aversive experience (the unconditioned stimulus (US), usually a shock) and a neutral stimulus (the conditioned stimulus (CS), usually an auditory cue or light flash)
Synonyms (1)
"impaired cued fear conditioning" EXACT
Parents (1)
img abnormal cued conditioning behavior MP:0001454
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053867img abnormal cued conditioning behavior MP:0001454
Genes (24)

Species:
human : 24
SpeciesGeneGeneIdGene NameEvidence
HumanNCF1653361neutrophil cytosolic factor 1
Click here to display 40 evidence detail records.
HumanARX170302aristaless related homeobox
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HumanPOMK84197protein-O-mannose kinase
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HumanEHMT179813euchromatic histone-lysine N-methyltransferase 1
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HumanNLGN354413neuroligin 3
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HumanNRN151299neuritin 1
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HumanGIT128964G protein-coupled receptor kinase interacting ArfGAP 1
Click here to display 40 evidence detail records.
HumanWWC123286WW and C2 domain containing 1
Click here to display 40 evidence detail records.
HumanKSR18844kinase suppressor of ras 1
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HumanSYNGAP18831synaptic Ras GTPase activating protein 1
Click here to display 40 evidence detail records.
HumanFZD37976frizzled family receptor 3
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HumanEIF4H7458eukaryotic translation initiation factor 4H
Click here to display 40 evidence detail records.
HumanTRPV17442transient receptor potential cation channel, subfamily V, member 1
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HumanCDKL56792cyclin-dependent kinase-like 5
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HumanMAPK15594mitogen-activated protein kinase 1
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HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
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HumanFMR12332fragile X mental retardation 1
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HumanFGF132258fibroblast growth factor 13
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HumanESR22100estrogen receptor 2 (ER beta)
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HumanERBB42066v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 4
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HumanDBN11627drebrin 1
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HumanCHRM31131cholinergic receptor, muscarinic 3
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HumanCAMK4814calcium/calmodulin-dependent protein kinase IV
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HumanBDNF627brain-derived neurotrophic factor
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XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009456impaired cued conditioning behavior0self