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Details
Link-It Detail - Jax Mouse Phenotype - cochlear hair cell degeneration
Debug Stats
  • ### Total Build Time: 197 ms 29.903 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 282 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 191 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= 1.024 KB
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.043 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 9.699 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=170 ms Completed: 170 ms rowSize= 15.980 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
cochlear hair cell degeneration MP:0004362
Definition (1)
degeneration or loss of the sensory epithelial cells of the cochlea; these cells are in synaptic contact with the auditory nerve
Synonyms (1)
"auditory hair cell degeneration" RELATED
Parents (2)
img abnormal cochlear hair cell morphology MP:0002622
img neuron degeneration MP:0003224
Children (2)
img cochlear inner hair cell degeneration MP:0004398
img cochlear outer hair cell degeneration MP:0004404
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal cochlear hair cell morphology MP:0002622
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img abnormal cochlear hair cell morphology MP:0002622
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053777img abnormal cochlear hair cell morphology MP:0002622
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053778img abnormal cochlear hair cell morphology MP:0002622
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img abnormal cochlear hair cell morphology MP:0002622
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537710img abnormal cochlear hair cell morphology MP:0002622
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img neuron degeneration MP:0003224
Genes (70)

Species:
human : 70
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
Click here to display 72 evidence detail records.
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
Click here to display 72 evidence detail records.
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
Click here to display 72 evidence detail records.
HumanTMIE259236transmembrane inner ear
Click here to display 72 evidence detail records.
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
Click here to display 72 evidence detail records.
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanSYNE4163183spectrin repeat containing, nuclear envelope family member 4
INFERRED
HumanLOXHD1125336lipoxygenase homology domains 1
Click here to display 72 evidence detail records.
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
Click here to display 72 evidence detail records.
HumanSRRM484530serine/arginine repetitive matrix 4
INFERRED
HumanGPR9884059G protein-coupled receptor 98
Click here to display 72 evidence detail records.
HumanESPN83715espin
Click here to display 72 evidence detail records.
HumanTMPRSS364699transmembrane protease, serine 3
Click here to display 72 evidence detail records.
HumanCDH2364072cadherin-related 23
Click here to display 72 evidence detail records.
HumanBARHL156751BarH-like homeobox 1
INFERRED
HumanMYO3A53904myosin IIIA
INFERRED
HumanCLIC553405chloride intracellular channel 5
INFERRED
HumanFBXO226232F-box protein 2
Click here to display 72 evidence detail records.
HumanDFNB3125861deafness, autosomal recessive 31
INFERRED
HumanCLDN1423562claudin 14
Click here to display 72 evidence detail records.
HumanSUN123353Sad1 and UNC84 domain containing 1
INFERRED
HumanGJB610804gap junction protein, beta 6, 30kDa
Click here to display 72 evidence detail records.
HumanSLC12A710723solute carrier family 12 (potassium/chloride transporter), member 7
INFERRED
HumanSLC19A210560solute carrier family 19 (thiamine transporter), member 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004362cochlear hair cell degeneration0self