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Details
Link-It Detail - Jax Mouse Phenotype - abnormal object recognition memory
Debug Stats
  • ### Total Build Time: 150 ms 21.252 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 445 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 197 bytes
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  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=6 ms Completed: 6 ms rowSize= 592 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.058 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.590 KB
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  • CONCEPT_GENES gt=134 ms Completed: 134 ms rowSize= 15.696 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal object recognition memory MP:0001458
Definition (1)
anomaly in the ability to recognize objects that the animal has previously encountered; recognition is measured by relative amount of time exploring objects, which should decrease upon subsequent or multiple presentations of the same object when presented with novel objects at the same time
Synonyms (1)
"object recognition memory abnormalities" EXACT
Parents (1)
img abnormal learning/memory/conditioning MP:0002063
Children (2)
img abnormal long term object recognition memory MP:0002801
img abnormal short term object recognition memory MP:0002800
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053865img abnormal learning/memory/conditioning MP:0002063
Genes (48)

Species:
human : 48
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanFOXO6100132074forkhead box O6
INFERRED
HumanNHLRC1378884NHL repeat containing 1
Click here to display 39 evidence detail records.
HumanEHMT179813euchromatic histone-lysine N-methyltransferase 1
Click here to display 39 evidence detail records.
HumanCARF79800calcium responsive transcription factor
Click here to display 39 evidence detail records.
HumanKIF1757576kinesin family member 17
INFERRED
HumanJPH357338junctophilin 3
INFERRED
HumanSLC17A757030solute carrier family 17 (vesicular glutamate transporter), member 7
INFERRED
HumanDCDC251473doublecortin domain containing 2
INFERRED
HumanFZR151343fizzy/cell division cycle 20 related 1 (Drosophila)
Click here to display 39 evidence detail records.
HumanGAL51083galanin/GMAP prepropeptide
Click here to display 39 evidence detail records.
HumanGIT128964G protein-coupled receptor kinase interacting ArfGAP 1
Click here to display 39 evidence detail records.
HumanKCNH323416potassium voltage-gated channel, subfamily H (eag-related), member 3
INFERRED
HumanARC23237activity-regulated cytoskeleton-associated protein
INFERRED
HumanTNIK23043TRAF2 and NCK interacting kinase
Click here to display 39 evidence detail records.
HumanRGS1410636regulator of G-protein signaling 14
INFERRED
HumanBAIAP210458BAI1-associated protein 2
Click here to display 39 evidence detail records.
HumanSRGAP39901SLIT-ROBO Rho GTPase activating protein 3
INFERRED
HumanNCOR19611nuclear receptor corepressor 1
INFERRED
HumanITM2B9445integral membrane protein 2B
Click here to display 39 evidence detail records.
HumanKL9365klotho
INFERRED
HumanWASF18936WAS protein family, member 1
Click here to display 39 evidence detail records.
HumanHDAC38841histone deacetylase 3
INFERRED
HumanTHRA7067thyroid hormone receptor, alpha
Click here to display 39 evidence detail records.
HumanSLC18A36572solute carrier family 18 (vesicular acetylcholine transporter), member 3
Click here to display 39 evidence detail records.
HumanSLC18A16570solute carrier family 18 (vesicular monoamine transporter), member 1
Click here to display 39 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001458abnormal object recognition memory0self