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Details
Link-It Detail - Jax Mouse Phenotype - cochlear ganglion degeneration
Debug Stats
  • ### Total Build Time: 243 ms 22.910 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 287 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 189 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=3 ms Completed: 3 ms rowSize= 592 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.932 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=228 ms Completed: 228 ms rowSize= 17.236 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
cochlear ganglion degeneration MP:0002857
Definition (1)
loss of neural cell bodies in the group of nerve cell bodies that conveys auditory sensation from the organ of Corti to the hindbrain
Synonyms (1)
"degeneration of spiral ganglion" EXACT
Parents (1)
img abnormal cochlear ganglion morphology MP:0002855
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img abnormal cochlear ganglion morphology MP:0002855
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal cochlear ganglion morphology MP:0002855
Genes (45)

Species:
human : 45
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Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
Click here to display 84 evidence detail records.
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
Click here to display 84 evidence detail records.
HumanTMIE259236transmembrane inner ear
Click here to display 84 evidence detail records.
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
Click here to display 84 evidence detail records.
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
Click here to display 84 evidence detail records.
HumanLOXHD1125336lipoxygenase homology domains 1
Click here to display 84 evidence detail records.
HumanSRRM484530serine/arginine repetitive matrix 4
Click here to display 84 evidence detail records.
HumanGPR9884059G protein-coupled receptor 98
Click here to display 84 evidence detail records.
HumanTMPRSS364699transmembrane protease, serine 3
Click here to display 84 evidence detail records.
HumanCDH2364072cadherin-related 23
Click here to display 84 evidence detail records.
HumanELMOD155531ELMO/CED-12 domain containing 1
Click here to display 84 evidence detail records.
HumanCLIC553405chloride intracellular channel 5
Click here to display 84 evidence detail records.
HumanFBXO226232F-box protein 2
Click here to display 84 evidence detail records.
HumanSLC12A710723solute carrier family 12 (potassium/chloride transporter), member 7
Click here to display 84 evidence detail records.
HumanUSH1C10083Usher syndrome 1C (autosomal recessive, severe)
Click here to display 84 evidence detail records.
HumanSLC12A69990solute carrier family 12 (potassium/chloride transporter), member 6
Click here to display 84 evidence detail records.
HumanS1PR29294sphingosine-1-phosphate receptor 2
Click here to display 84 evidence detail records.
HumanRGN9104regucalcin
Click here to display 84 evidence detail records.
HumanAP3D18943adaptor-related protein complex 3, delta 1 subunit
Click here to display 84 evidence detail records.
HumanSYNJ28871synaptojanin 2
Click here to display 84 evidence detail records.
HumanTUB7275tubby bipartite transcription factor
Click here to display 84 evidence detail records.
HumanSOD16647superoxide dismutase 1, soluble
Click here to display 84 evidence detail records.
HumanSLC9A16548solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1
Click here to display 84 evidence detail records.
HumanPOU4F35459POU class 4 homeobox 3
Click here to display 84 evidence detail records.
HumanNGFR4804nerve growth factor receptor
Click here to display 84 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002857cochlear ganglion degeneration0self