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Details
Link-It Detail - Jax Mouse Phenotype - deafness
Debug Stats
  • ### Total Build Time: 622 ms 21.728 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 344 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 263 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 179 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=4 ms Completed: 4 ms rowSize= 571 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.570 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=601 ms Completed: 601 ms rowSize= 17.533 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
deafness MP:0001967
Definition (1)
inability to hear; the ability to detect and/or recognize certain frequencies of sound is completely impaired
Synonyms (1)
"complete hearing loss" EXACT
Parents (1)
img impaired hearing MP:0006325
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053776img impaired hearing MP:0006325
Genes (76)

Species:
human : 76
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Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
Click here to display 228 evidence detail records.
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
Click here to display 228 evidence detail records.
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
Click here to display 228 evidence detail records.
HumanTMIE259236transmembrane inner ear
Click here to display 228 evidence detail records.
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
Click here to display 228 evidence detail records.
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
Click here to display 228 evidence detail records.
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
Click here to display 228 evidence detail records.
HumanOTOS150677otospiralin
Click here to display 228 evidence detail records.
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
Click here to display 228 evidence detail records.
HumanTMC1117531transmembrane channel-like 1
Click here to display 228 evidence detail records.
HumanGPR9884059G protein-coupled receptor 98
Click here to display 228 evidence detail records.
HumanESPN83715espin
Click here to display 228 evidence detail records.
HumanTMPRSS364699transmembrane protease, serine 3
Click here to display 228 evidence detail records.
HumanCDH2364072cadherin-related 23
Click here to display 228 evidence detail records.
HumanBARHL156751BarH-like homeobox 1
Click here to display 228 evidence detail records.
HumanELMOD155531ELMO/CED-12 domain containing 1
Click here to display 228 evidence detail records.
HumanMCOLN355283mucolipin 3
Click here to display 228 evidence detail records.
HumanCLIC553405chloride intracellular channel 5
Click here to display 228 evidence detail records.
HumanMYO15A51168myosin XVA
Click here to display 228 evidence detail records.
HumanFGF2026281fibroblast growth factor 20
Click here to display 228 evidence detail records.
HumanFBXO226232F-box protein 2
Click here to display 228 evidence detail records.
HumanCLDN1423562claudin 14
Click here to display 228 evidence detail records.
HumanTRIOBP11078TRIO and F-actin binding protein
Click here to display 228 evidence detail records.
HumanGJB610804gap junction protein, beta 6, 30kDa
Click here to display 228 evidence detail records.
HumanSLC12A710723solute carrier family 12 (potassium/chloride transporter), member 7
Click here to display 228 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001967deafness0self