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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cochlear ganglion morphology
Debug Stats
  • ### Total Build Time: 49 ms 22.199 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 402 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 370 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 181 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 1.038 KB
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.474 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 2.929 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=27 ms Completed: 27 ms rowSize= 14.509 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cochlear ganglion morphology MP:0002855
Definition (1)
any structural anomaly of the group of nerve cell bodies that conveys auditory sensation from the organ of Corti to the hindbrain and resides on the cochlear part of the vestibulocochlear nerve (eighth cranial nerve)
Synonyms (1)
"abnormal Corti ganglion" EXACT
Parents (2)
img abnormal sensory ganglion morphology MP:0000960
img abnormal cranial ganglia morphology MP:0001081
Children (3)
img small cochlear ganglion MP:0003986
img absent cochlear ganglion MP:0003146
img cochlear ganglion degeneration MP:0002857
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal sensory ganglion morphology MP:0000960
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal cranial ganglia morphology MP:0001081
Genes (67)

Species:
human : 67
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanTMIE259236transmembrane inner ear
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
Click here to display 23 evidence detail records.
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanCYS1192668cystin 1
INFERRED
HumanLOXHD1125336lipoxygenase homology domains 1
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
INFERRED
HumanSLITRK684189SLIT and NTRK-like family, member 6
INFERRED
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
INFERRED
HumanCDH2364072cadherin-related 23
Click here to display 23 evidence detail records.
HumanHR55806hair growth associated
INFERRED
HumanELMOD155531ELMO/CED-12 domain containing 1
INFERRED
HumanCLIC553405chloride intracellular channel 5
INFERRED
HumanFBXO226232F-box protein 2
INFERRED
HumanSLC12A710723solute carrier family 12 (potassium/chloride transporter), member 7
INFERRED
HumanUSH1C10083Usher syndrome 1C (autosomal recessive, severe)
INFERRED
HumanSLC12A69990solute carrier family 12 (potassium/chloride transporter), member 6
INFERRED
HumanS1PR29294sphingosine-1-phosphate receptor 2
INFERRED
HumanRGN9104regucalcin
INFERRED
HumanAP3D18943adaptor-related protein complex 3, delta 1 subunit
INFERRED
HumanSYNJ28871synaptojanin 2
INFERRED
HumanTUB7275tubby bipartite transcription factor
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002855abnormal cochlear ganglion morphology0self