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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cochlear hair bundle ankle links morphology
Debug Stats
  • ### Total Build Time: 11 ms 13.455 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 432 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 621 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= 618 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 596 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 8.517 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 1.391 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.189 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cochlear hair bundle ankle links morphology MP:0004581
Definition (1)
any structural anomaly in the long, single-stranded filaments that form a dense web or mesh around the base of cochlear hair bundles just above the region in which the stereocilia begin to taper down; in the mouse, ankle links are only a transient feature of the developing cochlear hair bundles, present predominantly from P2 though P9, but are absent by P12; ankle links are disrupted by treatment of hair cells with EGTA and subtilisin but not by La3+ and elastase
Parents (1)
img abnormal cochlear hair cell inter-stereocilial links morphology MP:0004577
Children (1)
img absent cochlear hair bundle ankle links MP:0004582
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img abnormal cochlear hair cell inter-stereocilial links morphology MP:0004577
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363112img abnormal cochlear hair cell inter-stereocilial links morphology MP:0004577
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img abnormal cochlear hair cell inter-stereocilial links morphology MP:0004577
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537710img abnormal cochlear hair cell inter-stereocilial links morphology MP:0004577
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537711img abnormal cochlear hair cell inter-stereocilial links morphology MP:0004577
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537712img abnormal cochlear hair cell inter-stereocilial links morphology MP:0004577
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanMYO7A4647myosin VIIA
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004581abnormal cochlear hair bundle ankle links morphology0self