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Details
Link-It Detail - Jax Mouse Phenotype - cochlear inner hair cell degeneration
Debug Stats
  • ### Total Build Time: 294 ms 38.240 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 402 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 255 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=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=31 ms Completed: 31 ms rowSize= 1.042 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 17.843 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=247 ms Completed: 247 ms rowSize= 17.196 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
cochlear inner hair cell degeneration MP:0004398
Definition (1)
degeneration or loss of the single row of flask-shaped inner hair sensory cells of the organ of Corti
Synonyms (1)
"auditory inner hair cell degeneration" EXACT
Parents (2)
img abnormal cochlear inner hair cell morphology MP:0004393
img cochlear hair cell degeneration MP:0004362
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img abnormal cochlear inner hair cell morphology MP:0004393
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img abnormal cochlear inner hair cell morphology MP:0004393
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053778img abnormal cochlear inner hair cell morphology MP:0004393
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img abnormal cochlear inner hair cell morphology MP:0004393
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537710img abnormal cochlear inner hair cell morphology MP:0004393
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537711img abnormal cochlear inner hair cell morphology MP:0004393
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img 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 cochlear hair cell degeneration MP:0004362
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537711img cochlear hair cell degeneration MP:0004362
Genes (41)

Species:
human : 41
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
Click here to display 66 evidence detail records.
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
Click here to display 66 evidence detail records.
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
Click here to display 66 evidence detail records.
HumanTMC1117531transmembrane channel-like 1
Click here to display 66 evidence detail records.
HumanSRRM484530serine/arginine repetitive matrix 4
Click here to display 66 evidence detail records.
HumanGPR9884059G protein-coupled receptor 98
Click here to display 66 evidence detail records.
HumanESPN83715espin
Click here to display 66 evidence detail records.
HumanTMPRSS364699transmembrane protease, serine 3
Click here to display 66 evidence detail records.
HumanBARHL156751BarH-like homeobox 1
Click here to display 66 evidence detail records.
HumanMYO3A53904myosin IIIA
Click here to display 66 evidence detail records.
HumanCLIC553405chloride intracellular channel 5
Click here to display 66 evidence detail records.
HumanDFNB3125861deafness, autosomal recessive 31
Click here to display 66 evidence detail records.
HumanCLDN1423562claudin 14
Click here to display 66 evidence detail records.
HumanSLC19A210560solute carrier family 19 (thiamine transporter), member 2
Click here to display 66 evidence detail records.
HumanUSH1C10083Usher syndrome 1C (autosomal recessive, severe)
Click here to display 66 evidence detail records.
HumanSLC12A69990solute carrier family 12 (potassium/chloride transporter), member 6
Click here to display 66 evidence detail records.
HumanSYNJ28871synaptojanin 2
Click here to display 66 evidence detail records.
HumanFZD48322frizzled family receptor 4
Click here to display 66 evidence detail records.
HumanTUB7275tubby bipartite transcription factor
Click here to display 66 evidence detail records.
HumanSOD16647superoxide dismutase 1, soluble
Click here to display 66 evidence detail records.
HumanSLC1A36507solute carrier family 1 (glial high affinity glutamate transporter), member 3
Click here to display 66 evidence detail records.
HumanPOU4F35459POU class 4 homeobox 3
Click here to display 66 evidence detail records.
HumanATP8B15205ATPase, aminophospholipid transporter, class I, type 8B, member 1
Click here to display 66 evidence detail records.
HumanSLC26A45172solute carrier family 26 (anion exchanger), member 4
Click here to display 66 evidence detail records.
HumanNDP4693Norrie disease (pseudoglioma)
Click here to display 66 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004398cochlear inner hair cell degeneration0self