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Details
Link-It Detail - Jax Mouse Phenotype - absent cochlear microphonics
Debug Stats
  • ### Total Build Time: 74 ms 43.979 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 384 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 269 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 183 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=3 ms Completed: 3 ms rowSize= 585 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=24 ms Completed: 24 ms rowSize= 2.927 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=36 ms Completed: 36 ms rowSize= 38.346 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
absent cochlear microphonics MP:0004413
Definition (1)
absence or loss of the bioelectric potentials produced by the hair cells of the organ of Corti in response to sound
Synonyms (1)
"absent cochlear potential" EXACT
Parents (1)
img abnormal cochlear microphonics MP:0004412
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img abnormal cochlear microphonics MP:0004412
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053778img abnormal cochlear microphonics MP:0004412
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:2450757
img Jax MP, Pubmed Id: 6871029, MOUSE PHENOTYPE ID: MGI:1861630
img Jax MP, Pubmed Id: 9435277, MOUSE PHENOTYPE ID: MGI:104510
img Jax MP, Pubmed Id: 12239568, MOUSE PHENOTYPE ID: MGI:1933154
img Jax MP, Pubmed Id: 22539951, MOUSE PHENOTYPE ID: MGI:2444748
img Jax MP, Pubmed Id: 9183385, MOUSE PHENOTYPE ID: MGI:107756
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
img Jax MP, Pubmed Id: 9183385, MOUSE PHENOTYPE ID: MGI:107756
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:2450757
img Jax MP, Pubmed Id: 22539951, MOUSE PHENOTYPE ID: MGI:2444748
img Jax MP, Pubmed Id: 6871029, MOUSE PHENOTYPE ID: MGI:1861630
img Jax MP, Pubmed Id: 9435277, MOUSE PHENOTYPE ID: MGI:104510
img Jax MP, Pubmed Id: 12239568, MOUSE PHENOTYPE ID: MGI:1933154
HumanESPN83715espin
img Jax MP, Pubmed Id: 9435277, MOUSE PHENOTYPE ID: MGI:104510
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
img Jax MP, Pubmed Id: 22539951, MOUSE PHENOTYPE ID: MGI:2444748
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
img Jax MP, Pubmed Id: 12239568, MOUSE PHENOTYPE ID: MGI:1933154
img Jax MP, Pubmed Id: 6871029, MOUSE PHENOTYPE ID: MGI:1861630
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:2450757
img Jax MP, Pubmed Id: 9183385, MOUSE PHENOTYPE ID: MGI:107756
HumanCHD755636chromodomain helicase DNA binding protein 7
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
img Jax MP, Pubmed Id: 12239568, MOUSE PHENOTYPE ID: MGI:1933154
img Jax MP, Pubmed Id: 9183385, MOUSE PHENOTYPE ID: MGI:107756
img Jax MP, Pubmed Id: 22539951, MOUSE PHENOTYPE ID: MGI:2444748
img Jax MP, Pubmed Id: 9435277, MOUSE PHENOTYPE ID: MGI:104510
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
img Jax MP, Pubmed Id: 6871029, MOUSE PHENOTYPE ID: MGI:1861630
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:2450757
HumanMYO15A51168myosin XVA
img Jax MP, Pubmed Id: 9183385, MOUSE PHENOTYPE ID: MGI:107756
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
img Jax MP, Pubmed Id: 12239568, MOUSE PHENOTYPE ID: MGI:1933154
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:2450757
img Jax MP, Pubmed Id: 6871029, MOUSE PHENOTYPE ID: MGI:1861630
img Jax MP, Pubmed Id: 9435277, MOUSE PHENOTYPE ID: MGI:104510
img Jax MP, Pubmed Id: 22539951, MOUSE PHENOTYPE ID: MGI:2444748
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
HumanMYO7A4647myosin VIIA
img Jax MP, Pubmed Id: 9435277, MOUSE PHENOTYPE ID: MGI:104510
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
img Jax MP, Pubmed Id: 9183385, MOUSE PHENOTYPE ID: MGI:107756
img Jax MP, Pubmed Id: 6871029, MOUSE PHENOTYPE ID: MGI:1861630
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:2450757
img Jax MP, Pubmed Id: 22539951, MOUSE PHENOTYPE ID: MGI:2444748
img Jax MP, Pubmed Id: 12239568, MOUSE PHENOTYPE ID: MGI:1933154
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004413absent cochlear microphonics0self