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Details
Link-It Detail - Jax Mouse Phenotype - cochlear degeneration
Debug Stats
  • ### Total Build Time: 119 ms 20.266 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 370 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 303 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=15 ms Completed: 15 ms rowSize= 1.480 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.581 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=67 ms Completed: 67 ms rowSize= 14.675 KB
  • CONCEPT_XREFS gt=9 ms Completed: 9 ms rowSize= 1.159 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
cochlear degeneration MP:0000032
Definition (1)
a retrogressive impairment of function or destruction of the spiral-shaped bony canal in the inner ear containing the hair cells that transduce sound
Parents (1)
img abnormal cochlea morphology MP:0000031
Children (3)
img stria vascularis degeneration MP:0004363
img organ of Corti degeneration MP:0000043
img spiral ligament degeneration MP:0004864
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053776img abnormal cochlea morphology MP:0000031
Genes (51)

Species:
human : 51
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
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
INFERRED
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanTMC1117531transmembrane channel-like 1
Click here to display 12 evidence detail records.
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanESPN83715espin
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
INFERRED
HumanCDH2364072cadherin-related 23
INFERRED
HumanELMOD155531ELMO/CED-12 domain containing 1
INFERRED
HumanCLIC553405chloride intracellular channel 5
INFERRED
HumanFBXO226232F-box protein 2
Click here to display 12 evidence detail records.
HumanGJB610804gap junction protein, beta 6, 30kDa
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
HumanSLC4A79497solute carrier family 4, sodium bicarbonate cotransporter, member 7
Click here to display 12 evidence detail records.
HumanS1PR29294sphingosine-1-phosphate receptor 2
INFERRED
HumanAP3D18943adaptor-related protein complex 3, delta 1 subunit
INFERRED
HumanSYNJ28871synaptojanin 2
INFERRED
HumanFZD48322frizzled family receptor 4
INFERRED
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED
HumanCLRN17401clarin 1
INFERRED
HumanTUB7275tubby bipartite transcription factor
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000032cochlear degeneration0self