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Details
Link-It Detail - Jax Mouse Phenotype - abnormal locomotor activation
Debug Stats
  • ### Total Build Time: 368 ms 24.858 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 223 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=2 ms Completed: 2 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 5.424 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.580 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=356 ms Completed: 356 ms rowSize= 15.380 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal locomotor activation MP:0003313
Definition (1)
altered ability or desire of an animal to initiate locomotor activity
Parents (1)
img abnormal locomotor behavior MP:0001392
Children (12)
img no spontaneous movement MP:0001404
img retropulsion MP:0010323
img decreased vertical activity MP:0002757
img dystonia MP:0005323
img hyperactivity MP:0001399
img behavioral arrest MP:0008035
img lethargy MP:0005202
img akinesia MP:0002690
img increased vertical activity MP:0002574
img bradykinesia MP:0005156
img positive geotaxis MP:0005356
img hypoactivity MP:0001402
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053867img abnormal locomotor behavior MP:0001392
Genes (696)

Species:
human : 696
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanFOXO6100132074forkhead box O6
INFERRED
HumanNCF1653361neutrophil cytosolic factor 1
Click here to display 164 evidence detail records.
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanPLIN5440503perilipin 5
INFERRED
HumanBSX390259brain-specific homeobox
INFERRED
HumanAGRN375790agrin
INFERRED
HumanTBX10347853T-box 10
INFERRED
HumanLRRTM1347730leucine rich repeat transmembrane neuronal 1
INFERRED
HumanATXN1L342371ataxin 1-like
INFERRED
HumanOTOG340990otogelin
INFERRED
HumanHMX3340784H6 family homeobox 3
INFERRED
HumanNAT8L339983N-acetyltransferase 8-like (GCN5-related, putative)
INFERRED
HumanDOK7285489docking protein 7
INFERRED
HumanPTRF284119polymerase I and transcript release factor
INFERRED
HumanSLC13A5284111solute carrier family 13 (sodium-dependent citrate transporter), member 5
INFERRED
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
INFERRED
HumanNPAS4266743neuronal PAS domain protein 4
INFERRED
HumanNEGR1257194neuronal growth regulator 1
INFERRED
HumanLCLAT1253558lysocardiolipin acyltransferase 1
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanFOXK1221937forkhead box K1
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanFBXO45200933F-box protein 45
INFERRED
HumanPIKFYVE200576phosphoinositide kinase, FYVE finger containing
INFERRED
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003313abnormal locomotor activation0self