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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cochlea morphology
Debug Stats
  • ### Total Build Time: 421 ms 26.349 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 272 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 176 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=16 ms Completed: 16 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= 584 bytes
  • CONCEPT_CHILDREN gt=8 ms Completed: 8 ms rowSize= 6.986 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.583 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=392 ms Completed: 392 ms rowSize= 15.089 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal cochlea morphology MP:0000031
Definition (1)
any structural anomaly of the spiral-shaped bony canal in the inner ear containing the hair cells that transduce sound
Synonyms (1)
"cochlear dysplasia" EXACT
Parents (1)
img abnormal inner ear morphology MP:0000026
Children (15)
img cochlear degeneration MP:0000032
img absent cochlea MP:0003147
img abnormal spiral limbus morphology MP:0004287
img abnormal Boettcher cell morphology MP:0011739
img abnormal cochlear sensory epithelium morphology MP:0003308
img abnormal Reissner membrane morphology MP:0006021
img abnormal scala media morphology MP:0003169
img abnormal cochlear basement membrane morphology MP:0004598
img abnormal modiolus morphology MP:0003309
img abnormal scala tympani morphology MP:0003167
img decreased cochlear coiling MP:0003148
img abnormal basilar membrane morphology MP:0004308
img abnormal scala vestibuli morphology MP:0003168
img abnormal Rosenthal canal morphology MP:0004305
img dilated cochlea MP:0004493
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053775img abnormal inner ear morphology MP:0000026
Genes (197)

Species:
human : 197
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
Click here to display 86 evidence detail records.
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
Click here to display 86 evidence detail records.
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:0000031abnormal cochlea morphology0self