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Details
Link-It Detail - Jax Mouse Phenotype - abnormal distortion product otoacoustic emission
Debug Stats
  • ### Total Build Time: 50 ms 20.522 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 424 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 367 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 175 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= 584 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 604 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.583 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=41 ms Completed: 41 ms rowSize= 15.506 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.186 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal distortion product otoacoustic emission MP:0004736
Definition (1)
any abnormality in the sound produced by the cochlea in response to stimulation with 2 simultaneous tones of different frequencies; this measurement is particularly useful in assessing the functional state of OHCs
Synonyms (1)
"abnormal DPOAE(s)" EXACT
Parents (1)
img abnormal otoacoustic response MP:0006336
Children (1)
img absent distortion product otoacoustic emissions MP:0004737
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053776img abnormal otoacoustic response MP:0006336
Genes (49)

Species:
human : 49
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCEACAM16388551carcinoembryonic antigen-related cell adhesion molecule 16
Click here to display 43 evidence detail records.
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanSTRC161497stereocilin
INFERRED
HumanLOXHD1125336lipoxygenase homology domains 1
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
Click here to display 43 evidence detail records.
HumanSRRM484530serine/arginine repetitive matrix 4
Click here to display 43 evidence detail records.
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
INFERRED
HumanCDH2364072cadherin-related 23
Click here to display 43 evidence detail records.
HumanCHRNA1057053cholinergic receptor, nicotinic, alpha 10 (neuronal)
Click here to display 43 evidence detail records.
HumanCHD755636chromodomain helicase DNA binding protein 7
Click here to display 43 evidence detail records.
HumanCHRNA955584cholinergic receptor, nicotinic, alpha 9 (neuronal)
Click here to display 43 evidence detail records.
HumanSOBP55084sine oculis binding protein homolog (Drosophila)
INFERRED
HumanMYO15A51168myosin XVA
INFERRED
HumanDFNB3125861deafness, autosomal recessive 31
INFERRED
HumanSLC19A210560solute carrier family 19 (thiamine transporter), member 2
Click here to display 43 evidence detail records.
HumanS1PR29294sphingosine-1-phosphate receptor 2
INFERRED
HumanKCNQ49132potassium voltage-gated channel, KQT-like subfamily, member 4
INFERRED
HumanMKKS8195McKusick-Kaufman syndrome
INFERRED
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED
HumanCLRN17401clarin 1
INFERRED
HumanUSH2A7399Usher syndrome 2A (autosomal recessive, mild)
Click here to display 43 evidence detail records.
HumanUCN7349urocortin
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XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004736abnormal distortion product otoacoustic emission0self