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Details
Link-It Detail - Jax Mouse Phenotype - abnormal behavior
Debug Stats
  • ### Total Build Time: 1,252 ms 27.205 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 362 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 287 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 185 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=0 Completed: 0 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=33 ms Completed: 33 ms rowSize= 7.411 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.584 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=1,202 ms Completed: 1.202 Seconds rowSize= 15.523 KB
  • CONCEPT_XREFS gt=9 ms Completed: 9 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal behavior MP:0004924
Definition (1)
any anomaly in the actions, reactions, or performance of an organism in response to external or internal stimuli compared to controls
Synonyms (1)
"abnormal general behavior" RELATED
Parents (1)
img behavior/neurological phenotype MP:0005386
Children (16)
img abnormal grooming behavior MP:0001440
img abnormal sleep behavior MP:0011396
img abnormal motor capabilities/coordination/movement MP:0002066
img catalepsy MP:0002822
img abnormal circadian rhythm MP:0001502
img abnormal consumption behavior MP:0002069
img abnormal behavioral response to xenobiotic MP:0009745
img abnormal emotion/affect behavior MP:0002572
img abnormal learning/memory/conditioning MP:0002063
img abnormal behavioral response to light MP:0011275
img abnormal sensory capabilities/reflexes/nociception MP:0002067
img seizures MP:0002064
img fatigue MP:0002899
img abnormal vocalization MP:0001529
img abnormal impulsive behavior control MP:0010698
img abnormal social/conspecific interaction MP:0002557
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053863img behavior/neurological phenotype MP:0005386
Genes (2002)

Species:
human : 2002
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMINOS1-NBL1100532736
INFERRED
HumanCOMMD3-BMI1100532731
INFERRED
HumanCASP12100506742caspase 12 (gene/pseudogene)
INFERRED
HumanOCLN100506658occludin
INFERRED
HumanTIMM23100287932translocase of inner mitochondrial membrane 23 homolog (yeast)
INFERRED
HumanFOXO6100132074forkhead box O6
INFERRED
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED
HumanSKOR2652991SKI family transcriptional corepressor 2
INFERRED
HumanPIRT644139phosphoinositide-interacting regulator of transient receptor potential channels
INFERRED
HumanCBLN3643866cerebellin 3 precursor
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanMBOAT4619373membrane bound O-acyltransferase domain containing 4
INFERRED
HumanSPRN503542shadow of prion protein homolog (zebrafish)
INFERRED
HumanDFNB59494513deafness, autosomal recessive 59
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanTRIM72493829tripartite motif containing 72
INFERRED
HumanPLIN5440503perilipin 5
INFERRED
HumanUNC13C440279unc-13 homolog C (C. elegans)
INFERRED
HumanEIF2AK4440275eukaryotic translation initiation factor 2 alpha kinase 4
INFERRED
HumanLHX8431707LIM homeobox 8
INFERRED
HumanCCL3L3414062chemokine (C-C motif) ligand 3-like 3
INFERRED
HumanGRID2IP392862glutamate receptor, ionotropic, delta 2 (Grid2) interacting protein
INFERRED
HumanHELT391723helt bHLH transcription factor
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004924abnormal behavior0self