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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cochlear endolymph
Debug Stats
  • ### Total Build Time: 50 ms 13.909 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 274 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=10 ms Completed: 10 ms rowSize= 573 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 588 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 1.572 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 9.253 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cochlear endolymph MP:0006390
Definition (1)
change in the normal production (volume) or ionic homeostasis of the fluid contained within the cochlea of the inner ear
Parents (1)
img abnormal endolymph MP:0004885
Children (1)
img abnormal endocochlear potential MP:0002630
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053775img abnormal endolymph MP:0004885
Genes (19)

Species:
human : 19
SpeciesGeneGeneIdGene NameEvidence
HumanSLC4A1183959solute carrier family 4, sodium borate transporter, member 11
INFERRED
HumanESPN83715espin
INFERRED
HumanFBXO1180204F-box protein 11
INFERRED
HumanATP6V0A450617ATPase, H+ transporting, lysosomal V0 subunit a4
INFERRED
HumanGJB610804gap junction protein, beta 6, 30kDa
INFERRED
HumanSLC12A69990solute carrier family 12 (potassium/chloride transporter), member 6
INFERRED
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED
HumanTYRP17306tyrosinase-related protein 1
INFERRED
HumanTHRA7067thyroid hormone receptor, alpha
INFERRED
HumanPOU3F45456POU class 3 homeobox 4
INFERRED
HumanSLC26A45172solute carrier family 26 (anion exchanger), member 4
INFERRED
HumanCLDN115010claudin 11
INFERRED
HumanNEUROD14760neuronal differentiation 1
INFERRED
HumanKIT3815v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
INFERRED
HumanKCNJ103766potassium inwardly-rectifying channel, subfamily J, member 10
INFERRED
HumanGRID12894glutamate receptor, ionotropic, delta 1
INFERRED
HumanFOXI12299forkhead box I1
INFERRED
HumanFGFR12260fibroblast growth factor receptor 1
INFERRED
HumanSCARB2950scavenger receptor class B, member 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006390abnormal cochlear endolymph0self