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Details
Link-It Detail - Jax Mouse Phenotype - stria vascularis degeneration
Debug Stats
  • ### Total Build Time: 24 ms 13.605 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 330 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
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  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 1.024 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.287 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=19 ms Completed: 19 ms rowSize= 6.275 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
stria vascularis degeneration MP:0004363
Definition (1)
degeneration or loss of the stratified, secretory epithelium which lines the upper part of the cochlear spiral ligament and maintains potassium ion homeostasis in the endolymph
Parents (2)
img cochlear degeneration MP:0000032
img abnormal stria vascularis morphology MP:0000048
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053777img cochlear degeneration MP:0000032
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053778img abnormal stria vascularis morphology MP:0000048
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img abnormal stria vascularis morphology MP:0000048
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
Click here to display 17 evidence detail records.
HumanFZD48322frizzled family receptor 4
Click here to display 17 evidence detail records.
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
Click here to display 17 evidence detail records.
HumanPOU4F35459POU class 4 homeobox 3
Click here to display 17 evidence detail records.
HumanPOLG5428polymerase (DNA directed), gamma
Click here to display 17 evidence detail records.
HumanSLC26A45172solute carrier family 26 (anion exchanger), member 4
Click here to display 17 evidence detail records.
HumanNDP4693Norrie disease (pseudoglioma)
Click here to display 17 evidence detail records.
HumanMYO7A4647myosin VIIA
Click here to display 17 evidence detail records.
HumanMYO64646myosin VI
Click here to display 17 evidence detail records.
HumanLAMA23908laminin, alpha 2
Click here to display 17 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004363stria vascularis degeneration0self