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Details
Link-It Detail - Jax Mouse Phenotype - abnormal ear physiology
Debug Stats
  • ### Total Build Time: 31 ms 23.150 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 374 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 220 bytes
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  • 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
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  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 3.765 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.586 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=28 ms Completed: 28 ms rowSize= 15.341 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.161 KB
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Jax Mouse Phenotype (1)
abnormal ear physiology MP:0003878
Definition (1)
any functional anomaly of the ear, not due to an anatomical defect
Parents (1)
img hearing/vestibular/ear phenotype MP:0005377
Children (8)
img abnormal hair cell physiology MP:0003879
img abnormal vestibular system physiology MP:0004742
img abnormal perilymph MP:0004888
img abnormal hearing physiology MP:0001963
img abnormal blood-inner ear barrier function MP:0004999
img ear inflammation MP:0001849
img abnormal organ of Corti supporting cell physiology MP:0008305
img abnormal endolymph MP:0004885
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053773img hearing/vestibular/ear phenotype MP:0005377
Genes (252)

Species:
human : 252
Page Size
Current 25
  Page 1 of 11
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDFNB59494513deafness, autosomal recessive 59
INFERRED
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanCEACAM16388551carcinoembryonic antigen-related cell adhesion molecule 16
INFERRED
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
INFERRED
HumanGJC3349149gap junction protein, gamma 3, 30.2kDa
INFERRED
HumanOTOG340990otogelin
Click here to display 12 evidence detail records.
HumanSH3PXD2B285590SH3 and PX domains 2B
INFERRED
HumanTMIE259236transmembrane inner ear
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanCYS1192668cystin 1
INFERRED
HumanSYNE4163183spectrin repeat containing, nuclear envelope family member 4
INFERRED
HumanSTRC161497stereocilin
INFERRED
HumanOTOS150677otospiralin
INFERRED
HumanOTOA146183otoancorin
INFERRED
HumanOTOP1133060otopetrin 1
INFERRED
HumanGIPC3126326GIPC PDZ domain containing family, member 3
INFERRED
HumanLOXHD1125336lipoxygenase homology domains 1
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC2117532transmembrane channel-like 2
INFERRED
HumanTMC1117531transmembrane channel-like 1
INFERRED
HumanNTNG284628netrin G2
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003878abnormal ear physiology0self