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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cochlear hair cell stereociliary bundle morphology
Debug Stats
  • ### Total Build Time: 104 ms 30.360 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 446 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 392 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 197 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=0 Completed: 0 ms rowSize= 593 bytes
  • CONCEPT_CHILDREN gt=10 ms Completed: 10 ms rowSize= 3.919 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 8.367 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=83 ms Completed: 83 ms rowSize= 15.144 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.196 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cochlear hair cell stereociliary bundle morphology MP:0004521
Definition (1)
any structural anomaly or disruption of the typical pattern of arrangement of mechanosensitive hair bundles which are composed of thick long microvilli (stereocilia) and are located at the apical end of cochlear inner and outer hair cells
Synonyms (1)
"abnormal cochlear hair cell stereocilia" EXACT
Parents (1)
img abnormal cochlear hair cell morphology MP:0002622
Children (8)
img abnormal orientation of cochlear hair cell stereociliary bundles MP:0004522
img decreased cochlear hair cell stereocilia number MP:0004523
img absent cochlear hair cell stereocilia MP:0004526
img abnormal outer hair cell stereociliary bundle morphology MP:0004527
img abnormal inner hair cell stereociliary bundle morphology MP:0004532
img short cochlear hair cell stereocilia MP:0004524
img thin cochlear hair cell stereocilia MP:0004525
img abnormal cochlear hair cell inter-stereocilial links morphology MP:0004577
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
Genes (64)

Species:
human : 64
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
Click here to display 37 evidence detail records.
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
Click here to display 37 evidence detail records.
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanSTRC161497stereocilin
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
INFERRED
HumanMOB1B92597MOB kinase activator 1B
INFERRED
HumanGPR9884059G protein-coupled receptor 98
Click here to display 37 evidence detail records.
HumanESPN83715espin
Click here to display 37 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
INFERRED
HumanVANGL257216VANGL planar cell polarity protein 2
Click here to display 37 evidence detail records.
HumanHR55806hair growth associated
INFERRED
HumanELMOD155531ELMO/CED-12 domain containing 1
Click here to display 37 evidence detail records.
HumanMKS154903Meckel syndrome, type 1
INFERRED
HumanCLIC553405chloride intracellular channel 5
Click here to display 37 evidence detail records.
HumanMYO15A51168myosin XVA
INFERRED
HumanDLL128514delta-like 1 (Drosophila)
INFERRED
HumanDFNB3125861deafness, autosomal recessive 31
Click here to display 37 evidence detail records.
HumanFSCN225794fascin homolog 2, actin-bundling protein, retinal (Strongylocentrotus purpuratus)
INFERRED
HumanCLDN1423562claudin 14
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004521abnormal cochlear hair cell stereociliary bundle morphology0self