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Details
Link-It Detail - Jax Mouse Phenotype - abnormal spatial working memory
Debug Stats
  • ### Total Build Time: 415 ms 21.514 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 360 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 170 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 592 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.590 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=392 ms Completed: 392 ms rowSize= 17.126 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal spatial working memory MP:0008428
Definition (1)
anomaly in the ability to spontaneously process spatial location information in order to navigate or perform other behavior using such location cues, without previous encounters or training at that location
Synonyms (1)
"abnormal SWM" EXACT
Parents (1)
img abnormal learning/memory/conditioning MP:0002063
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053865img abnormal learning/memory/conditioning MP:0002063
Genes (47)

Species:
human : 47
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Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanLRRTM1347730leucine rich repeat transmembrane neuronal 1
Click here to display 88 evidence detail records.
HumanSPRED1161742sprouty-related, EVH1 domain containing 1
Click here to display 88 evidence detail records.
HumanTANC185461tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1
Click here to display 88 evidence detail records.
HumanATAD184896ATPase family, AAA domain containing 1
Click here to display 88 evidence detail records.
HumanDGCR854487DGCR8 microprocessor complex subunit
Click here to display 88 evidence detail records.
HumanDCDC251473doublecortin domain containing 2
Click here to display 88 evidence detail records.
HumanSHANK150944SH3 and multiple ankyrin repeat domains 1
Click here to display 88 evidence detail records.
HumanDISC127185disrupted in schizophrenia 1
Click here to display 88 evidence detail records.
HumanFOXB127023forkhead box B1
Click here to display 88 evidence detail records.
HumanBACE123621beta-site APP-cleaving enzyme 1
Click here to display 88 evidence detail records.
HumanKCNH323416potassium voltage-gated channel, subfamily H (eag-related), member 3
Click here to display 88 evidence detail records.
HumanNCSTN23385nicastrin
Click here to display 88 evidence detail records.
HumanCHL110752cell adhesion molecule L1-like
Click here to display 88 evidence detail records.
HumanCERS110715ceramide synthase 1
Click here to display 88 evidence detail records.
HumanARL6IP510550ADP-ribosylation-like factor 6 interacting protein 5
Click here to display 88 evidence detail records.
HumanSRGAP39901SLIT-ROBO Rho GTPase activating protein 3
Click here to display 88 evidence detail records.
HumanITM2B9445integral membrane protein 2B
Click here to display 88 evidence detail records.
HumanKALRN8997kalirin, RhoGEF kinase
Click here to display 88 evidence detail records.
HumanSYNGAP18831synaptic Ras GTPase activating protein 1
Click here to display 88 evidence detail records.
HumanCUL4B8450cullin 4B
Click here to display 88 evidence detail records.
HumanTUBA1A7846tubulin, alpha 1a
Click here to display 88 evidence detail records.
HumanEIF4H7458eukaryotic translation initiation factor 4H
Click here to display 88 evidence detail records.
HumanTLR37098toll-like receptor 3
Click here to display 88 evidence detail records.
HumanTBX16899T-box 1
Click here to display 88 evidence detail records.
HumanSLC6A86535solute carrier family 6 (neurotransmitter transporter), member 8
Click here to display 88 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008428abnormal spatial working memory0self