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Details
Link-It Detail - Jax Mouse Phenotype - abnormal brain wave pattern
Debug Stats
  • ### Total Build Time: 435 ms 21.899 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 429 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 179 bytes
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  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=9 ms Completed: 9 ms rowSize= 596 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=8 ms Completed: 8 ms rowSize= 1.587 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=405 ms Completed: 405 ms rowSize= 17.446 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal brain wave pattern MP:0004994
Definition (1)
any anomaly in the standard pattern of rhythmic and rapid fluctuation of electrical potential between parts of the brain, often visualized on an electroencephalogram (EEG); the pattern is often measured to diagnose neurological conditions such as seizure disorders (epilepsy)
Synonyms (1)
"abnormal ECoG pattern" EXACT
Parents (1)
img abnormal nervous system electrophysiology MP:0002272
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img abnormal nervous system electrophysiology MP:0002272
Genes (49)

Species:
human : 49
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SpeciesGeneGeneIdGene NameEvidence
HumanFOXO6100132074forkhead box O6
Click here to display 81 evidence detail records.
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
Click here to display 81 evidence detail records.
HumanARX170302aristaless related homeobox
Click here to display 81 evidence detail records.
HumanGJD257369gap junction protein, delta 2, 36kDa
Click here to display 81 evidence detail records.
HumanGIT128964G protein-coupled receptor kinase interacting ArfGAP 1
Click here to display 81 evidence detail records.
HumanCNTNAP226047contactin associated protein-like 2
Click here to display 81 evidence detail records.
HumanRAI110743retinoic acid induced 1
Click here to display 81 evidence detail records.
HumanCACNG210369calcium channel, voltage-dependent, gamma subunit 2
Click here to display 81 evidence detail records.
HumanGABBR29568gamma-aminobutyric acid (GABA) B receptor, 2
Click here to display 81 evidence detail records.
HumanS1PR29294sphingosine-1-phosphate receptor 2
Click here to display 81 evidence detail records.
HumanCACNA2D29254calcium channel, voltage-dependent, alpha 2/delta subunit 2
Click here to display 81 evidence detail records.
HumanLGI19211leucine-rich, glioma inactivated 1
Click here to display 81 evidence detail records.
HumanAP3D18943adaptor-related protein complex 3, delta 1 subunit
Click here to display 81 evidence detail records.
HumanBSN8927bassoon presynaptic cytomatrix protein
Click here to display 81 evidence detail records.
HumanPER38863period circadian clock 3
Click here to display 81 evidence detail records.
HumanEPM2A7957epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
Click here to display 81 evidence detail records.
HumanALDH5A17915aldehyde dehydrogenase 5 family, member A1
Click here to display 81 evidence detail records.
HumanUBE3A7337ubiquitin protein ligase E3A
Click here to display 81 evidence detail records.
HumanTSC17248tuberous sclerosis 1
Click here to display 81 evidence detail records.
HumanTNFRSF1A7132tumor necrosis factor receptor superfamily, member 1A
Click here to display 81 evidence detail records.
HumanSSTR26752somatostatin receptor 2
Click here to display 81 evidence detail records.
HumanSSTR16751somatostatin receptor 1
Click here to display 81 evidence detail records.
HumanSLC2A36515solute carrier family 2 (facilitated glucose transporter), member 3
Click here to display 81 evidence detail records.
HumanSCN10A6336sodium channel, voltage-gated, type X, alpha subunit
Click here to display 81 evidence detail records.
HumanSCN1B6324sodium channel, voltage-gated, type I, beta subunit
Click here to display 81 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004994abnormal brain wave pattern0self