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Details
Link-It Detail - Jax Mouse Phenotype - abnormal organ of Corti morphology
Debug Stats
  • ### Total Build Time: 544 ms 24.317 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 396 bytes
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  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 190 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 3.336 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.936 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=517 ms Completed: 517 ms rowSize= 15.257 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal organ of Corti morphology MP:0000042
Definition (1)
any structural anomaly associated with the highly specialized epithelium in the floor of the ductus cochlearis; also referred to a spiral organ (organum spirale), or acoustic papilla
Synonyms (1)
"abnormal spiral organ morphology" EXACT
Parents (1)
img abnormal scala media morphology MP:0003169
Children (7)
img abnormal cuticular plate morphology MP:0010015
img abnormal patterning of the organ of Corti MP:0006331
img absent organ of Corti MP:0000044
img organ of Corti degeneration MP:0000043
img abnormal cochlear hair cell morphology MP:0002622
img abnormal organ of Corti supporting cell morphology MP:0004300
img absent tunnel of Corti MP:0003151
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053777img abnormal scala media morphology MP:0003169
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053778img abnormal scala media morphology MP:0003169
Genes (157)

Species:
human : 157
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanHES5388585hairy and enhancer of split 5 (Drosophila)
INFERRED
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
INFERRED
HumanTMIE259236transmembrane inner ear
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanCYS1192668cystin 1
Click here to display 65 evidence detail records.
HumanSYNE4163183spectrin repeat containing, nuclear envelope family member 4
INFERRED
HumanSTRC161497stereocilin
INFERRED
HumanOTOA146183otoancorin
INFERRED
HumanLOXHD1125336lipoxygenase homology domains 1
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
INFERRED
HumanCTHRC1115908collagen triple helix repeat containing 1
INFERRED
HumanMOB1B92597MOB kinase activator 1B
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
INFERRED
HumanSLITRK684189SLIT and NTRK-like family, member 6
INFERRED
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanESPN83715espin
Click here to display 65 evidence detail records.
HumanVANGL181839VANGL planar cell polarity protein 1
INFERRED
HumanFAT479633FAT atypical cadherin 4
INFERRED
HumanSMURF264750SMAD specific E3 ubiquitin protein ligase 2
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
Click here to display 65 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000042abnormal organ of Corti morphology0self