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Details
Link-It Detail - Jax Mouse Phenotype - abnormal hearing electrophysiology
Debug Stats
  • ### Total Build Time: 22 ms 22.811 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 220 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
  • 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=0 Completed: 0 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 3.354 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.581 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 15.390 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal hearing electrophysiology MP:0006335
Definition (1)
anomaly in auditory function as it relates to electrical phenomena
Parents (1)
img abnormal hearing physiology MP:0001963
Children (7)
img abnormal auditory summating potential MP:0006388
img abnormal cochlear nerve fiber response MP:0006324
img abnormal cochlear nerve compound action potential MP:0004415
img abnormal endocochlear potential MP:0002630
img abnormal auditory brainstem response MP:0004738
img abnormal cochlear frequency tuning MP:0006383
img abnormal cochlear potential MP:0006332
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053775img abnormal hearing physiology MP:0001963
Genes (174)

Species:
human : 174
Page Size
Current 25
  Page 1 of 7
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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
HumanGJC3349149gap junction protein, gamma 3, 30.2kDa
INFERRED
HumanOTOG340990otogelin
INFERRED
HumanSH3PXD2B285590SH3 and PX domains 2B
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
Click here to display 8 evidence detail records.
HumanOTOS150677otospiralin
INFERRED
HumanOTOA146183otoancorin
INFERRED
HumanGIPC3126326GIPC PDZ domain containing family, member 3
INFERRED
HumanLOXHD1125336lipoxygenase homology domains 1
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
INFERRED
HumanNTNG284628netrin G2
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
Click here to display 8 evidence detail records.
HumanSLITRK684189SLIT and NTRK-like family, member 6
INFERRED
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanSLC4A1183959solute carrier family 4, sodium borate transporter, member 11
INFERRED
HumanESPN83715espin
Click here to display 8 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006335abnormal hearing electrophysiology0self