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Details
Link-It Detail - Jax Mouse Phenotype - absence seizures
Debug Stats
  • ### Total Build Time: 54 ms 22.188 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 360 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 348 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 177 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=0 Completed: 0 ms rowSize= 577 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 586 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.909 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=45 ms Completed: 45 ms rowSize= 15.979 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.154 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
absence seizures MP:0003216
Definition (1)
impairment of consciousness without convulsions associated with sudden behavioral arrest and widespread bilaterally synchronous spike-and-wave discharges (SWDs) in the electroencephalogram (EEG)
Synonyms (1)
"spike wave seizures" EXACT
Parents (1)
img nonconvulsive seizures MP:0000948
Children (1)
img abnormal spike wave discharge MP:0008840
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img nonconvulsive seizures MP:0000948
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053866img nonconvulsive seizures MP:0000948
Genes (31)

Species:
human : 31
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNHLRC1378884NHL repeat containing 1
INFERRED
HumanSLC10A4201780solute carrier family 10, member 4
INFERRED
HumanARX170302aristaless related homeobox
INFERRED
HumanCELF456853CUGBP, Elav-like family member 4
Click here to display 42 evidence detail records.
HumanLHX626468LIM homeobox 6
INFERRED
HumanKCNH323416potassium voltage-gated channel, subfamily H (eag-related), member 3
INFERRED
HumanCACNG210369calcium channel, voltage-dependent, gamma subunit 2
Click here to display 42 evidence detail records.
HumanHDAC49759histone deacetylase 4
INFERRED
HumanCACNA2D29254calcium channel, voltage-dependent, alpha 2/delta subunit 2
Click here to display 42 evidence detail records.
HumanLGI19211leucine-rich, glioma inactivated 1
INFERRED
HumanAP3D18943adaptor-related protein complex 3, delta 1 subunit
INFERRED
HumanCACNA1G8913calcium channel, voltage-dependent, T type, alpha 1G subunit
INFERRED
HumanALDH5A17915aldehyde dehydrogenase 5 family, member A1
Click here to display 42 evidence detail records.
HumanUBE3A7337ubiquitin protein ligase E3A
Click here to display 42 evidence detail records.
HumanTEF7008thyrotrophic embryonic factor
Click here to display 42 evidence detail records.
HumanSLC9A16548solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1
Click here to display 42 evidence detail records.
HumanSCN8A6334sodium channel, voltage gated, type VIII, alpha subunit
INFERRED
HumanSCN1A6323sodium channel, voltage-gated, type I, alpha subunit
INFERRED
HumanPTEN5728phosphatase and tensin homolog
INFERRED
HumanGRIA42893glutamate receptor, ionotropic, AMPA 4
Click here to display 42 evidence detail records.
HumanGRIA32892glutamate receptor, ionotropic, AMPA 3
Click here to display 42 evidence detail records.
HumanGABRG22566gamma-aminobutyric acid (GABA) A receptor, gamma 2
Click here to display 42 evidence detail records.
HumanGABRD2563gamma-aminobutyric acid (GABA) A receptor, delta
Click here to display 42 evidence detail records.
HumanGABRA12554gamma-aminobutyric acid (GABA) A receptor, alpha 1
Click here to display 42 evidence detail records.
HumanGABBR12550gamma-aminobutyric acid (GABA) B receptor, 1
Click here to display 42 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003216absence seizures0self