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Details
Link-It Detail - Jax Mouse Phenotype - cochlear outer hair cell degeneration
Debug Stats
  • ### Total Build Time: 300 ms 38.467 KB
  • CONCEPT_NAME gt=10 ms Completed: 10 ms rowSize= 402 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 237 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 195 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=5 ms Completed: 5 ms rowSize= 1.042 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=12 ms Completed: 12 ms rowSize= 17.843 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=272 ms Completed: 272 ms rowSize= 17.440 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
cochlear outer hair cell degeneration MP:0004404
Definition (1)
degeneration or loss of the columnar outer hair sensory cells of the organ of Corti
Synonyms (1)
"auditory outer hair cell degeneration" EXACT
Parents (2)
img cochlear hair cell degeneration MP:0004362
img abnormal cochlear outer hair cell morphology MP:0004399
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img cochlear hair cell degeneration MP:0004362
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537710img cochlear hair cell degeneration MP:0004362
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537711img cochlear hair cell degeneration MP:0004362
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img cochlear hair cell degeneration MP:0004362
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img cochlear hair cell degeneration MP:0004362
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053778img cochlear hair cell degeneration MP:0004362
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img cochlear hair cell degeneration MP:0004362
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537710img abnormal cochlear outer hair cell morphology MP:0004399
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537711img abnormal cochlear outer hair cell morphology MP:0004399
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img abnormal cochlear outer hair cell morphology MP:0004399
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img abnormal cochlear outer hair cell morphology MP:0004399
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053778img abnormal cochlear outer hair cell morphology MP:0004399
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img abnormal cochlear outer hair cell morphology MP:0004399
Genes (55)

Species:
human : 55
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Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
Click here to display 101 evidence detail records.
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
Click here to display 101 evidence detail records.
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
Click here to display 101 evidence detail records.
HumanSYNE4163183spectrin repeat containing, nuclear envelope family member 4
Click here to display 101 evidence detail records.
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
Click here to display 101 evidence detail records.
HumanTMC1117531transmembrane channel-like 1
Click here to display 101 evidence detail records.
HumanGPR9884059G protein-coupled receptor 98
Click here to display 101 evidence detail records.
HumanESPN83715espin
Click here to display 101 evidence detail records.
HumanTMPRSS364699transmembrane protease, serine 3
Click here to display 101 evidence detail records.
HumanCDH2364072cadherin-related 23
Click here to display 101 evidence detail records.
HumanBARHL156751BarH-like homeobox 1
Click here to display 101 evidence detail records.
HumanMYO3A53904myosin IIIA
Click here to display 101 evidence detail records.
HumanCLIC553405chloride intracellular channel 5
Click here to display 101 evidence detail records.
HumanDFNB3125861deafness, autosomal recessive 31
Click here to display 101 evidence detail records.
HumanCLDN1423562claudin 14
Click here to display 101 evidence detail records.
HumanSUN123353Sad1 and UNC84 domain containing 1
Click here to display 101 evidence detail records.
HumanSLC12A710723solute carrier family 12 (potassium/chloride transporter), member 7
Click here to display 101 evidence detail records.
HumanSLC19A210560solute carrier family 19 (thiamine transporter), member 2
Click here to display 101 evidence detail records.
HumanUSH1C10083Usher syndrome 1C (autosomal recessive, severe)
Click here to display 101 evidence detail records.
HumanSLC12A69990solute carrier family 12 (potassium/chloride transporter), member 6
Click here to display 101 evidence detail records.
HumanCELSR19620cadherin, EGF LAG seven-pass G-type receptor 1
Click here to display 101 evidence detail records.
HumanS1PR29294sphingosine-1-phosphate receptor 2
Click here to display 101 evidence detail records.
HumanKCNQ49132potassium voltage-gated channel, KQT-like subfamily, member 4
Click here to display 101 evidence detail records.
HumanCLDN99080claudin 9
Click here to display 101 evidence detail records.
HumanSYNJ28871synaptojanin 2
Click here to display 101 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004404cochlear outer hair cell degeneration0self