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Details
Link-It Detail - Jax Mouse Phenotype - abnormal inner ear vestibule morphology
Debug Stats
  • ### Total Build Time: 53 ms 20.757 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 406 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 255 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 202 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
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 584 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.961 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.583 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=47 ms Completed: 47 ms rowSize= 14.479 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.177 KB
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Jax Mouse Phenotype (1)
abnormal inner ear vestibule morphology MP:0000034
Definition (1)
any structural anomaly of the cavity between the semicircular canals and the cochlea of the inner ear
Synonyms (1)
"abnormal bony labyrinth vestibule morphology" EXACT
Parents (1)
img abnormal inner ear morphology MP:0000026
Children (4)
img abnormal vestibular dark cell morphology MP:0004775
img absent inner ear vestibule MP:0004314
img abnormal vestibular hair cell morphology MP:0002623
img abnormal otolith organ morphology MP:0004425
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053775img abnormal inner ear morphology MP:0000026
Genes (66)

Species:
human : 66
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanOC90729330otoconin 90
INFERRED
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanHES5388585hairy and enhancer of split 5 (Drosophila)
Click here to display 33 evidence detail records.
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
INFERRED
HumanTBX10347853T-box 10
Click here to display 33 evidence detail records.
HumanOTOG340990otogelin
INFERRED
HumanHMX3340784H6 family homeobox 3
INFERRED
HumanTMIE259236transmembrane inner ear
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
INFERRED
HumanCDH2364072cadherin-related 23
INFERRED
HumanVANGL257216VANGL planar cell polarity protein 2
INFERRED
HumanCLIC553405chloride intracellular channel 5
INFERRED
HumanDLL128514delta-like 1 (Drosophila)
INFERRED
HumanATG4B23192autophagy related 4B, cysteine peptidase
INFERRED
HumanCACNG210369calcium channel, voltage-dependent, gamma subunit 2
INFERRED
HumanUSH1C10083Usher syndrome 1C (autosomal recessive, severe)
INFERRED
HumanATG59474autophagy related 5
INFERRED
HumanS1PR29294sphingosine-1-phosphate receptor 2
INFERRED
HumanAP3D18943adaptor-related protein complex 3, delta 1 subunit
Click here to display 33 evidence detail records.
HumanITGA88516integrin, alpha 8
INFERRED
HumanZEB16935zinc finger E-box binding homeobox 1
INFERRED
HumanTBX16899T-box 1
INFERRED
HumanSOX26657SRY (sex determining region Y)-box 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000034abnormal inner ear vestibule morphology0self