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Details
Link-It Detail - Jax Mouse Phenotype - abnormal orientation of outer hair cell stereociliary bundles
Debug Stats
  • ### Total Build Time: 38 ms 31.981 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 450 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 308 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 1.086 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 16.765 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=30 ms Completed: 30 ms rowSize= 12.040 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.198 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal orientation of outer hair cell stereociliary bundles MP:0004491
Definition (1)
misorientation or rotation of outer hair cell (OHC) stereociliary bundles, resulting in defective planar cell polarity of the inner ear sensory epithelium
Parents (2)
img abnormal orientation of cochlear hair cell stereociliary bundles MP:0004522
img abnormal outer hair cell stereociliary bundle morphology MP:0004527
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img abnormal orientation of cochlear hair cell stereociliary bundles MP:0004522
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363112img abnormal orientation of cochlear hair cell stereociliary bundles MP:0004522
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img abnormal orientation of cochlear hair cell stereociliary bundles MP:0004522
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537710img abnormal orientation of cochlear hair cell stereociliary bundles MP:0004522
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537711img abnormal orientation of cochlear hair cell stereociliary bundles MP:0004522
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537712img abnormal orientation of cochlear hair cell stereociliary bundles MP:0004522
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img abnormal outer hair cell stereociliary bundle morphology MP:0004527
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363112img abnormal outer hair cell stereociliary bundle morphology MP:0004527
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img abnormal outer hair cell stereociliary bundle morphology MP:0004527
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537710img abnormal outer hair cell stereociliary bundle morphology MP:0004527
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537711img abnormal outer hair cell stereociliary bundle morphology MP:0004527
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537712img abnormal outer hair cell stereociliary bundle morphology MP:0004527
Genes (20)

Species:
human : 20
SpeciesGeneGeneIdGene NameEvidence
HumanGPR9884059G protein-coupled receptor 98
Click here to display 38 evidence detail records.
HumanFAT479633FAT atypical cadherin 4
Click here to display 38 evidence detail records.
HumanSMURF264750SMAD specific E3 ubiquitin protein ligase 2
Click here to display 38 evidence detail records.
HumanCDH2364072cadherin-related 23
Click here to display 38 evidence detail records.
HumanVANGL257216VANGL planar cell polarity protein 2
Click here to display 38 evidence detail records.
HumanMKS154903Meckel syndrome, type 1
Click here to display 38 evidence detail records.
HumanSEC24B10427SEC24 family, member B (S. cerevisiae)
Click here to display 38 evidence detail records.
HumanUSH1C10083Usher syndrome 1C (autosomal recessive, severe)
Click here to display 38 evidence detail records.
HumanCELSR19620cadherin, EGF LAG seven-pass G-type receptor 1
Click here to display 38 evidence detail records.
HumanDCHS18642dachsous 1 (Drosophila)
Click here to display 38 evidence detail records.
HumanFZD18321frizzled family receptor 1
Click here to display 38 evidence detail records.
HumanMKKS8195McKusick-Kaufman syndrome
Click here to display 38 evidence detail records.
HumanCLRN17401clarin 1
Click here to display 38 evidence detail records.
HumanNR2F17025nuclear receptor subfamily 2, group F, member 1
Click here to display 38 evidence detail records.
HumanPTK75754protein tyrosine kinase 7
Click here to display 38 evidence detail records.
HumanMYO7A4647myosin VIIA
Click here to display 38 evidence detail records.
HumanFZD22535frizzled family receptor 2
Click here to display 38 evidence detail records.
HumanDVL21856dishevelled segment polarity protein 2
Click here to display 38 evidence detail records.
HumanBBS4585Bardet-Biedl syndrome 4
Click here to display 38 evidence detail records.
HumanBBS1582Bardet-Biedl syndrome 1
Click here to display 38 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004491abnormal orientation of outer hair cell stereociliary bundles0self