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Details
Link-It Detail - Jax Mouse Phenotype - akinesia
Debug Stats
  • ### Total Build Time: 79 ms 15.697 KB
  • CONCEPT_NAME gt=7 ms Completed: 6 ms rowSize= 344 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 285 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 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=6 ms Completed: 6 ms rowSize= 584 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.582 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=60 ms Completed: 60 ms rowSize= 11.632 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
akinesia MP:0002690
Definition (1)
acquired absence of voluntary movement or loss of the ability to move such as temporary or prolonged paralysis or freezing in place
Parents (1)
img abnormal locomotor activation MP:0003313
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053868img abnormal locomotor activation MP:0003313
Genes (19)

Species:
human : 19
SpeciesGeneGeneIdGene NameEvidence
HumanDOK7285489docking protein 7
Click here to display 24 evidence detail records.
HumanSLC12A557468solute carrier family 12 (potassium/chloride transporter), member 5
Click here to display 24 evidence detail records.
HumanGPR12657211G protein-coupled receptor 126
Click here to display 24 evidence detail records.
HumanHTRA227429HtrA serine peptidase 2
Click here to display 24 evidence detail records.
HumanSLC12A69990solute carrier family 12 (potassium/chloride transporter), member 6
Click here to display 24 evidence detail records.
HumanLGI19211leucine-rich, glioma inactivated 1
Click here to display 24 evidence detail records.
HumanVAMP16843vesicle-associated membrane protein 1 (synaptobrevin 1)
Click here to display 24 evidence detail records.
HumanSNAP256616synaptosomal-associated protein, 25kDa
Click here to display 24 evidence detail records.
HumanSCN1A6323sodium channel, voltage-gated, type I, alpha subunit
Click here to display 24 evidence detail records.
HumanNR4A24929nuclear receptor subfamily 4, group A, member 2
Click here to display 24 evidence detail records.
HumanNBN4683nibrin
Click here to display 24 evidence detail records.
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
Click here to display 24 evidence detail records.
HumanMAP64135microtubule-associated protein 6
Click here to display 24 evidence detail records.
HumanINPP4A3631inositol polyphosphate-4-phosphatase, type I, 107kDa
Click here to display 24 evidence detail records.
HumanINS3630insulin
Click here to display 24 evidence detail records.
HumanGBA2629glucosidase, beta, acid
Click here to display 24 evidence detail records.
HumanDRD21813dopamine receptor D2
Click here to display 24 evidence detail records.
HumanDDC1644dopa decarboxylase (aromatic L-amino acid decarboxylase)
Click here to display 24 evidence detail records.
HumanDBH1621dopamine beta-hydroxylase (dopamine beta-monooxygenase)
Click here to display 24 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002690akinesia0self