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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cochlear microphonics
Debug Stats
  • ### Total Build Time: 289 ms 23.181 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 606 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=124 ms Completed: 124 ms rowSize= 1.038 KB
  • CONCEPT_CHILDREN gt=24 ms Completed: 24 ms rowSize= 1.028 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=77 ms Completed: 77 ms rowSize= 4.301 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=54 ms Completed: 54 ms rowSize= 14.530 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cochlear microphonics MP:0004412
Definition (1)
any anomaly in the bioelectric potentials produced by the hair cells of the organ of Corti in response to sound; the cochlear microphonic (CM) is an electric response dominated by OHC receptor potentials from the basal turn of the cochlea and provides a measure of transducer function in OHCs; in an active ear, CM waveforms show post-stimulus ringing (i.e. a cochlear echo) whereas in a passive ear system, CM decays at the cessation of the tone burst
Parents (2)
img abnormal cochlear potential MP:0006332
img abnormal cochlear outer hair cell physiology MP:0004434
Children (2)
img decreased cochlear microphonics MP:0004414
img absent cochlear microphonics MP:0004413
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053777img abnormal cochlear potential MP:0006332
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal cochlear outer hair cell physiology MP:0004434
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053777img abnormal cochlear outer hair cell physiology MP:0004434
Genes (12)

Species:
human : 12
SpeciesGeneGeneIdGene NameEvidence
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanSTRC161497stereocilin
img Jax MP, Pubmed Id: 11087000, MOUSE PHENOTYPE ID: MGI:109575
img Jax MP, Pubmed Id: 11124466, MOUSE PHENOTYPE ID: MGI:105368
img Jax MP, Pubmed Id: 18849963, MOUSE PHENOTYPE ID: MGI:2153816
img Jax MP, Pubmed Id: 20142329, MOUSE PHENOTYPE ID: MGI:109575
HumanOTOS150677otospiralin
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanESPN83715espin
INFERRED
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED
HumanMYO15A51168myosin XVA
INFERRED
HumanCLRN17401clarin 1
INFERRED
HumanTHRB7068thyroid hormone receptor, beta
INFERRED
HumanTECTA7007tectorin alpha
img Jax MP, Pubmed Id: 11087000, MOUSE PHENOTYPE ID: MGI:109575
img Jax MP, Pubmed Id: 18849963, MOUSE PHENOTYPE ID: MGI:2153816
img Jax MP, Pubmed Id: 11124466, MOUSE PHENOTYPE ID: MGI:105368
img Jax MP, Pubmed Id: 20142329, MOUSE PHENOTYPE ID: MGI:109575
HumanMYO7A4647myosin VIIA
INFERRED
HumanATP2B2491ATPase, Ca++ transporting, plasma membrane 2
img Jax MP, Pubmed Id: 18849963, MOUSE PHENOTYPE ID: MGI:2153816
img Jax MP, Pubmed Id: 20142329, MOUSE PHENOTYPE ID: MGI:109575
img Jax MP, Pubmed Id: 11087000, MOUSE PHENOTYPE ID: MGI:109575
img Jax MP, Pubmed Id: 11124466, MOUSE PHENOTYPE ID: MGI:105368
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004412abnormal cochlear microphonics0self