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Details
Link-It Detail - Jax Mouse Phenotype - decreased cochlear outer hair cell number
Debug Stats
  • ### Total Build Time: 26 ms 39.202 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 410 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 268 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 181 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=1 ms Completed: 1 ms rowSize= 1.042 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 589 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 19.195 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 16.228 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.179 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
decreased cochlear outer hair cell number MP:0004402
Definition (1)
decreased number (or less than the expected 3 rows) of the columnar outer hair sensory cells of the organ of Corti
Synonyms (1)
"decreased auditory OHCs" EXACT
Parents (2)
img abnormal cochlear outer hair cell number MP:0004400
img decreased cochlear hair cell number MP:0004408
Children (1)
img absent cochlear outer hair cells MP:0004403
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img abnormal cochlear outer hair cell number MP:0004400
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363112img abnormal cochlear outer hair cell number MP:0004400
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img abnormal cochlear outer hair cell number MP:0004400
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537710img abnormal cochlear outer hair cell number MP:0004400
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537711img abnormal cochlear outer hair cell number MP:0004400
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537712img abnormal cochlear outer hair cell number MP:0004400
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img decreased cochlear hair cell number MP:0004408
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363112img decreased cochlear hair cell number MP:0004408
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img decreased cochlear hair cell number MP:0004408
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537710img decreased cochlear hair cell number MP:0004408
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537711img decreased cochlear hair cell number MP:0004408
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537712img decreased cochlear hair cell number MP:0004408
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img decreased cochlear hair cell number MP:0004408
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img decreased cochlear hair cell number MP:0004408
Genes (28)

Species:
human : 28
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
Click here to display 27 evidence detail records.
HumanCYS1192668cystin 1
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
INFERRED
HumanCDH2364072cadherin-related 23
Click here to display 27 evidence detail records.
HumanHR55806hair growth associated
Click here to display 27 evidence detail records.
HumanMYO3A53904myosin IIIA
Click here to display 27 evidence detail records.
HumanFGF2026281fibroblast growth factor 20
Click here to display 27 evidence detail records.
HumanSLC12A710723solute carrier family 12 (potassium/chloride transporter), member 7
INFERRED
HumanCLDN99080claudin 9
Click here to display 27 evidence detail records.
HumanCLRN17401clarin 1
INFERRED
HumanUSH2A7399Usher syndrome 2A (autosomal recessive, mild)
Click here to display 27 evidence detail records.
HumanTSHR7253thyroid stimulating hormone receptor
Click here to display 27 evidence detail records.
HumanTHRB7068thyroid hormone receptor, beta
Click here to display 27 evidence detail records.
HumanSLC12A26558solute carrier family 12 (sodium/potassium/chloride transporter), member 2
Click here to display 27 evidence detail records.
HumanMYO7A4647myosin VIIA
Click here to display 27 evidence detail records.
HumanKCNE13753potassium voltage-gated channel, Isk-related family, member 1
INFERRED
HumanIGF1R3480insulin-like growth factor 1 receptor
Click here to display 27 evidence detail records.
HumanGFI12672growth factor independent 1 transcription repressor
Click here to display 27 evidence detail records.
HumanFOXG12290forkhead box G1
INFERRED
HumanFGFR12260fibroblast growth factor receptor 1
Click here to display 27 evidence detail records.
HumanEYA12138eyes absent homolog 1 (Drosophila)
Click here to display 27 evidence detail records.
HumanDVL31857dishevelled segment polarity protein 3
Click here to display 27 evidence detail records.
HumanDFNA51687deafness, autosomal dominant 5
Click here to display 27 evidence detail records.
HumanCOL11A11301collagen, type XI, alpha 1
INFERRED
HumanCDKN2D1032cyclin-dependent kinase inhibitor 2D (p19, inhibits CDK4)
Click here to display 27 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004402decreased cochlear outer hair cell number0self