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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cochlear labyrinth morphology
Debug Stats
  • ### Total Build Time: 65 ms 19.968 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 404 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 499 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 183 bytes
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  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 595 bytes
  • CONCEPT_CHILDREN gt=16 ms Completed: 16 ms rowSize= 588 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.594 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=44 ms Completed: 44 ms rowSize= 14.838 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.176 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cochlear labyrinth morphology MP:0004426
Definition (1)
any structural anomaly in the portion of the membranous labyrinth concerned with the sense of hearing (vs. the vestibular labyrinth, which is concerned with the sense of equilibration) and innervated by the cochlear nerve; it is located within the cochlea of the bony labyrinth, and consists of the cochlear duct, which contains the spiral organ
Synonyms (1)
"abnormal organ of hearing" EXACT
Parents (1)
img abnormal membranous labyrinth morphology MP:0000035
Children (1)
img abnormal scala media morphology MP:0003169
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053776img abnormal membranous labyrinth morphology MP:0000035
Genes (182)

Species:
human : 182
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)
INFERRED
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
INFERRED
HumanOTOG340990otogelin
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
HumanOTOS150677otospiralin
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
HumanSLC4A1183959solute carrier family 4, sodium borate transporter, member 11
INFERRED
HumanESPN83715espin
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004426abnormal cochlear labyrinth morphology0self