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Details
Link-It Detail - Jax Mouse Phenotype - vestibular hair cell degeneration
Debug Stats
  • ### Total Build Time: 96 ms 15.086 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 394 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 343 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
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  • CONCEPT_PARENTS gt=15 ms Completed: 15 ms rowSize= 1.026 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=31 ms Completed: 31 ms rowSize= 5.630 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=40 ms Completed: 40 ms rowSize= 6.387 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.171 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
vestibular hair cell degeneration MP:0004324
Definition (1)
degeneration or loss of the sensory epithelial cells of the maculae and cristae of the membranous labyrinth of the inner ear which are normally in synaptic contact with the vestibular nerve
Parents (2)
img neuron degeneration MP:0003224
img abnormal vestibular hair cell morphology MP:0002623
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img neuron degeneration MP:0003224
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img abnormal vestibular hair cell morphology MP:0002623
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal vestibular hair cell morphology MP:0002623
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053777img abnormal vestibular hair cell morphology MP:0002623
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
Click here to display 19 evidence detail records.
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
Click here to display 19 evidence detail records.
HumanTMPRSS364699transmembrane protease, serine 3
Click here to display 19 evidence detail records.
HumanCLIC553405chloride intracellular channel 5
Click here to display 19 evidence detail records.
HumanUSH1C10083Usher syndrome 1C (autosomal recessive, severe)
Click here to display 19 evidence detail records.
HumanSLC26A45172solute carrier family 26 (anion exchanger), member 4
Click here to display 19 evidence detail records.
HumanMYO64646myosin VI
Click here to display 19 evidence detail records.
HumanKIT3815v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
Click here to display 19 evidence detail records.
HumanKCNJ103766potassium inwardly-rectifying channel, subfamily J, member 10
Click here to display 19 evidence detail records.
HumanS1PR31903sphingosine-1-phosphate receptor 3
Click here to display 19 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004324vestibular hair cell degeneration0self