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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cochlear outer hair cell physiology
Debug Stats
  • ### Total Build Time: 83 ms 18.604 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 416 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 644 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 190 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 593 bytes
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 1.048 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=27 ms Completed: 27 ms rowSize= 2.941 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=27 ms Completed: 27 ms rowSize= 11.489 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.182 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cochlear outer hair cell physiology MP:0004434
Definition (1)
any functional anomaly in processes pertinent to the function of cochlear OHCs which are known to enhance the performance of the cochlea, both qualitatively (increased selectivity) and quantitatively (increased sensitivity); in addition to the mechanoelectric transduction required for auditory sensation, OHCs also perform electromechanical transduction, whereby transmembrane voltage drives rapid changes in the length and stiffness of OHCs at audio frequencies in vitro (electromotility)
Synonyms (1)
"abnormal cochlear OHC physiology" EXACT
Parents (1)
img abnormal cochlear hair cell physiology MP:0004432
Children (2)
img abnormal cochlear outer hair cell electromotility MP:0004435
img abnormal cochlear microphonics MP:0004412
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img abnormal cochlear hair cell physiology MP:0004432
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053776img abnormal cochlear hair cell physiology MP:0004432
Genes (21)

Species:
human : 21
SpeciesGeneGeneIdGene NameEvidence
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
Click here to display 17 evidence detail records.
HumanSTRC161497stereocilin
INFERRED
HumanOTOS150677otospiralin
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanGPR9884059G protein-coupled receptor 98
Click here to display 17 evidence detail records.
HumanESPN83715espin
INFERRED
HumanCDH2364072cadherin-related 23
Click here to display 17 evidence detail records.
HumanCHRNA1057053cholinergic receptor, nicotinic, alpha 10 (neuronal)
Click here to display 17 evidence detail records.
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED
HumanCHRNA955584cholinergic receptor, nicotinic, alpha 9 (neuronal)
Click here to display 17 evidence detail records.
HumanMYO15A51168myosin XVA
INFERRED
HumanKCNQ49132potassium voltage-gated channel, KQT-like subfamily, member 4
Click here to display 17 evidence detail records.
HumanCLRN17401clarin 1
INFERRED
HumanTHRB7068thyroid hormone receptor, beta
Click here to display 17 evidence detail records.
HumanTHRA7067thyroid hormone receptor, alpha
Click here to display 17 evidence detail records.
HumanTECTA7007tectorin alpha
Click here to display 17 evidence detail records.
HumanPSAP5660prosaposin
Click here to display 17 evidence detail records.
HumanMYO7A4647myosin VIIA
INFERRED
HumanHPN3249hepsin
Click here to display 17 evidence detail records.
HumanCACNA1D776calcium channel, voltage-dependent, L type, alpha 1D subunit
Click here to display 17 evidence detail records.
HumanATP2B2491ATPase, Ca++ transporting, plasma membrane 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004434abnormal cochlear outer hair cell physiology0self