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Details
Link-It Detail - Jax Mouse Phenotype - abnormal hair cell physiology
Debug Stats
  • ### Total Build Time: 23 ms 30.316 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 225 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 1.024 KB
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.521 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.923 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 22.940 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal hair cell physiology MP:0003879
Definition (1)
any functional anomaly of the sensory epithelial cells of the inner ear
Parents (2)
img abnormal sensory neuron physiology MP:0010055
img abnormal ear physiology MP:0003878
Children (3)
img abnormal cochlear hair cell physiology MP:0004432
img abnormal hair cell mechanoelectric transduction MP:0004431
img abnormal vestibular hair cell physiology MP:0004438
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal sensory neuron physiology MP:0010055
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053774img abnormal ear physiology MP:0003878
Genes (34)

Species:
human : 34
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanSTRC161497stereocilin
INFERRED
HumanOTOS150677otospiralin
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC2117532transmembrane channel-like 2
INFERRED
HumanTMC1117531transmembrane channel-like 1
img Jax MP, Pubmed Id: 19047635, MOUSE PHENOTYPE ID: MGI:3586899
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
img Jax MP, Pubmed Id: 19047635, MOUSE PHENOTYPE ID: MGI:107588
img Jax MP, Pubmed Id: 22105175, MOUSE PHENOTYPE ID: MGI:2151016
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanESPN83715espin
INFERRED
HumanCDH2364072cadherin-related 23
INFERRED
HumanCHRNA1057053cholinergic receptor, nicotinic, alpha 10 (neuronal)
INFERRED
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED
HumanCHRNA955584cholinergic receptor, nicotinic, alpha 9 (neuronal)
INFERRED
HumanMYO15A51168myosin XVA
img Jax MP, Pubmed Id: 22105175, MOUSE PHENOTYPE ID: MGI:2151016
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
img Jax MP, Pubmed Id: 19047635, MOUSE PHENOTYPE ID: MGI:107588
img Jax MP, Pubmed Id: 19047635, MOUSE PHENOTYPE ID: MGI:3586899
HumanTRIOBP11078TRIO and F-actin binding protein
INFERRED
HumanGJB610804gap junction protein, beta 6, 30kDa
img Jax MP, Pubmed Id: 19047635, MOUSE PHENOTYPE ID: MGI:3586899
img Jax MP, Pubmed Id: 22105175, MOUSE PHENOTYPE ID: MGI:2151016
img Jax MP, Pubmed Id: 19047635, MOUSE PHENOTYPE ID: MGI:107588
img Jax MP, Pubmed Id: 21436032, MOUSE PHENOTYPE ID: MGI:1261811
HumanUSH1C10083Usher syndrome 1C (autosomal recessive, severe)
INFERRED
HumanOTOF9381otoferlin
INFERRED
HumanKCNQ49132potassium voltage-gated channel, KQT-like subfamily, member 4
INFERRED
HumanCLRN17401clarin 1
INFERRED
HumanTHRB7068thyroid hormone receptor, beta
INFERRED
HumanTHRA7067thyroid hormone receptor, alpha
INFERRED
HumanTECTA7007tectorin alpha
INFERRED
HumanPSAP5660prosaposin
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003879abnormal hair cell physiology0self