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Details
Link-It Detail - Jax Mouse Phenotype - circling
Debug Stats
  • ### Total Build Time: 1,491 ms 21.978 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 344 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 224 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=2 ms Completed: 2 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 575 bytes
  • CONCEPT_CHILDREN gt=10 ms Completed: 10 ms rowSize= 1.015 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 1.573 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=1,448 ms Completed: 1.448 Seconds rowSize= 16.982 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
circling MP:0001394
Definition (1)
repeated movement in a circle; often associated with inner ear defects
Parents (1)
img stereotypic behavior MP:0001408
Children (2)
img unidirectional circling MP:0001396
img bidirectional circling MP:0001395
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053866img stereotypic behavior MP:0001408
Genes (85)

Species:
human : 85
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Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanDFNB59494513deafness, autosomal recessive 59
Click here to display 291 evidence detail records.
HumanGRXCR1389207glutaredoxin, cysteine rich 1
Click here to display 291 evidence detail records.
HumanTBX10347853T-box 10
INFERRED
HumanOTOG340990otogelin
Click here to display 291 evidence detail records.
HumanHMX3340784H6 family homeobox 3
Click here to display 291 evidence detail records.
HumanTMIE259236transmembrane inner ear
Click here to display 291 evidence detail records.
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
Click here to display 291 evidence detail records.
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
Click here to display 291 evidence detail records.
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
Click here to display 291 evidence detail records.
HumanLRIG3121227leucine-rich repeats and immunoglobulin-like domains 3
Click here to display 291 evidence detail records.
HumanTMC1117531transmembrane channel-like 1
Click here to display 291 evidence detail records.
HumanBTBD9114781BTB (POZ) domain containing 9
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
Click here to display 291 evidence detail records.
HumanESPN83715espin
Click here to display 291 evidence detail records.
HumanCDH2364072cadherin-related 23
Click here to display 291 evidence detail records.
HumanCHD755636chromodomain helicase DNA binding protein 7
Click here to display 291 evidence detail records.
HumanELMOD155531ELMO/CED-12 domain containing 1
Click here to display 291 evidence detail records.
HumanMCOLN355283mucolipin 3
Click here to display 291 evidence detail records.
HumanSOBP55084sine oculis binding protein homolog (Drosophila)
Click here to display 291 evidence detail records.
HumanCLIC553405chloride intracellular channel 5
INFERRED
HumanMYO15A51168myosin XVA
Click here to display 291 evidence detail records.
HumanATP6V0A450617ATPase, H+ transporting, lysosomal V0 subunit a4
Click here to display 291 evidence detail records.
HumanNOX350508NADPH oxidase 3
Click here to display 291 evidence detail records.
HumanNIPBL25836Nipped-B homolog (Drosophila)
Click here to display 291 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001394circling0self