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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cochlear hair cell morphology
Debug Stats
  • ### Total Build Time: 267 ms 30.481 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 404 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 284 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 209 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=10 ms Completed: 10 ms rowSize= 1.504 KB
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 2.925 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=16 ms Completed: 16 ms rowSize= 8.340 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=220 ms Completed: 220 ms rowSize= 15.517 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.176 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cochlear hair cell morphology MP:0002622
Definition (1)
any structural anomaly of the sensory epithelial cells of the cochlea; these cells are in synaptic contact with the auditory nerve
Synonyms (1)
"abnormal auditory hair cell morphology" EXACT [CL:0000202]
Parents (3)
img abnormal hair cell morphology MP:0000045
img abnormal cochlear sensory epithelium morphology MP:0003308
img abnormal organ of Corti morphology MP:0000042
Children (6)
img abnormal cochlear hair cell development MP:0004589
img cochlear hair cell degeneration MP:0004362
img abnormal cochlear inner hair cell morphology MP:0004393
img abnormal cochlear outer hair cell morphology MP:0004399
img abnormal cochlear hair cell number MP:0004406
img abnormal cochlear hair cell stereociliary bundle morphology MP:0004521
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img abnormal hair cell morphology MP:0000045
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal hair cell morphology MP:0000045
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053776img abnormal hair cell morphology MP:0000045
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053777img abnormal cochlear sensory epithelium morphology MP:0003308
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053778img abnormal organ of Corti morphology MP:0000042
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img abnormal organ of Corti morphology MP:0000042
Genes (149)

Species:
human : 149
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
INFERRED
HumanSYNE4163183spectrin repeat containing, nuclear envelope family member 4
INFERRED
HumanSTRC161497stereocilin
INFERRED
HumanLOXHD1125336lipoxygenase homology domains 1
Click here to display 47 evidence detail records.
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
INFERRED
HumanCTHRC1115908collagen triple helix repeat containing 1
Click here to display 47 evidence detail records.
HumanMOB1B92597MOB kinase activator 1B
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
INFERRED
HumanSLITRK684189SLIT and NTRK-like family, member 6
Click here to display 47 evidence detail records.
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanESPN83715espin
Click here to display 47 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
INFERRED
HumanCDH2364072cadherin-related 23
Click here to display 47 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002622abnormal cochlear hair cell morphology0self