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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cochlear inner hair cell morphology
Debug Stats
  • ### Total Build Time: 357 ms 30.190 KB
  • CONCEPT_NAME gt=21 ms Completed: 21 ms rowSize= 416 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 204 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 593 bytes
  • CONCEPT_CHILDREN gt=20 ms Completed: 20 ms rowSize= 3.416 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 8.367 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=289 ms Completed: 289 ms rowSize= 15.216 KB
  • CONCEPT_XREFS gt=20 ms Completed: 20 ms rowSize= 1.182 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cochlear inner hair cell morphology MP:0004393
Definition (1)
any structural anomaly in the sensory cells of the organ of Corti which are in synaptic contact with sensory as well as efferent fibers of the auditory nerve; there is a single row of flask-shaped inner hair cells tightly surrounded by supporting interphalangeal cells; the apical end of each cell is anchored to the cuticular plate and about 100 stereocilia arranged in a more or less linear (or shallow) U-shaped pattern extend from the cell's surface through the cuticular plate into the endolymphic space inferior to the tectorial membrane
Synonyms (1)
"abnormal auditory inner hair cell morphology" RELATED
Parents (1)
img abnormal cochlear hair cell morphology MP:0002622
Children (7)
img abnormal cochlear IHC efferent innervation pattern MP:0004633
img abnormal inner hair cell stereociliary bundle morphology MP:0004532
img abnormal cochlear inner hair cell number MP:0004394
img abnormal cochlear IHC afferent innervation pattern MP:0004746
img absent cochlear inner hair cells MP:0004397
img abnormal inner hair cell synaptic ribbon morphology MP:0004562
img cochlear inner hair cell degeneration MP:0004398
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053777img 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 nervous system phenotype MP:00036319img 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
Genes (98)

Species:
human : 98
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
Click here to display 37 evidence detail records.
HumanHES5388585hairy and enhancer of split 5 (Drosophila)
INFERRED
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
Click here to display 37 evidence detail records.
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanCYS1192668cystin 1
Click here to display 37 evidence detail records.
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
INFERRED
HumanCTHRC1115908collagen triple helix repeat containing 1
Click here to display 37 evidence detail records.
HumanMOB1B92597MOB kinase activator 1B
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
Click here to display 37 evidence detail records.
HumanSLITRK684189SLIT and NTRK-like family, member 6
INFERRED
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanESPN83715espin
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
INFERRED
HumanCDH2364072cadherin-related 23
INFERRED
HumanVANGL257216VANGL planar cell polarity protein 2
Click here to display 37 evidence detail records.
HumanCHRNA1057053cholinergic receptor, nicotinic, alpha 10 (neuronal)
INFERRED
HumanBARHL156751BarH-like homeobox 1
INFERRED
HumanHR55806hair growth associated
INFERRED
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED
HumanCHRNA955584cholinergic receptor, nicotinic, alpha 9 (neuronal)
INFERRED
HumanMYO3A53904myosin IIIA
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004393abnormal cochlear inner hair cell morphology0self