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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cochlear endolymph ionic homeostasis
Debug Stats
  • ### Total Build Time: 46 ms 14.938 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 418 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 469 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=13 ms Completed: 13 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=11 ms Completed: 11 ms rowSize= 1.585 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 10.580 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.183 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cochlear endolymph ionic homeostasis MP:0006403
Definition (1)
anomaly in the state of equilibrium in the cochlear endolymph with respect to charged molecules; cochlear endolymph is not only an unusual extracellular fluid for its high potassium ion and low sodium ion concentration but also for its low calcium ion concentration, high HCO3- concentration and low protein content
Parents (1)
img abnormal endocochlear potential MP:0002630
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053777img abnormal endocochlear potential MP:0002630
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanGJB610804gap junction protein, beta 6, 30kDa
img Jax MP, Pubmed Id: 12121617, MOUSE PHENOTYPE ID: MGI:2671942
img Jax MP, Pubmed Id: 17299139, MOUSE PHENOTYPE ID: MGI:1346029
img Jax MP, Pubmed Id: 12490528, MOUSE PHENOTYPE ID: MGI:107588
img Jax MP, Pubmed Id: 11788352, MOUSE PHENOTYPE ID: MGI:1194504
HumanSLC26A45172solute carrier family 26 (anion exchanger), member 4
img Jax MP, Pubmed Id: 12121617, MOUSE PHENOTYPE ID: MGI:2671942
img Jax MP, Pubmed Id: 17299139, MOUSE PHENOTYPE ID: MGI:1346029
img Jax MP, Pubmed Id: 12490528, MOUSE PHENOTYPE ID: MGI:107588
img Jax MP, Pubmed Id: 11788352, MOUSE PHENOTYPE ID: MGI:1194504
HumanKCNJ103766potassium inwardly-rectifying channel, subfamily J, member 10
img Jax MP, Pubmed Id: 12490528, MOUSE PHENOTYPE ID: MGI:107588
img Jax MP, Pubmed Id: 17299139, MOUSE PHENOTYPE ID: MGI:1346029
img Jax MP, Pubmed Id: 11788352, MOUSE PHENOTYPE ID: MGI:1194504
img Jax MP, Pubmed Id: 12121617, MOUSE PHENOTYPE ID: MGI:2671942
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006403abnormal cochlear endolymph ionic homeostasis0self