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Details
Link-It Detail - Jax Mouse Phenotype - abnormal auditory brainstem response
Debug Stats
  • ### Total Build Time: 240 ms 21.749 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 400 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 554 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 174 bytes
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  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 589 bytes
  • CONCEPT_CHILDREN gt=74 ms Completed: 74 ms rowSize= 1.558 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.588 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=151 ms Completed: 151 ms rowSize= 15.608 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.174 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal auditory brainstem response MP:0004738
Definition (1)
anomaly in the electrical activity generated in the ascending auditory system in response to short tone bursts; may be used to evaluate sensorineural hearing function; measurements may include the amplitude (the number of neurons firing), latency (the speed of transmission), interpeak latency (the time between peaks), interaural latency (the difference in wave V latency between ears) and threshold
Synonyms (1)
"abnormal BAEP(s)" EXACT
Parents (1)
img abnormal hearing electrophysiology MP:0006335
Children (3)
img decreased threshold for auditory brainstem response MP:0011968
img increased or absent threshold for auditory brainstem response MP:0011967
img abnormal auditory brainstem response waveform shape MP:0011966
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053776img abnormal hearing electrophysiology MP:0006335
Genes (158)

Species:
human : 158
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Current 25
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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
Click here to display 76 evidence detail records.
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
HumanGIPC3126326GIPC PDZ domain containing family, member 3
INFERRED
HumanLOXHD1125336lipoxygenase homology domains 1
Click here to display 76 evidence detail records.
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
INFERRED
HumanNTNG284628netrin G2
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
INFERRED
HumanSLITRK684189SLIT and NTRK-like family, member 6
INFERRED
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanSLC4A1183959solute carrier family 4, sodium borate transporter, member 11
Click here to display 76 evidence detail records.
HumanESPN83715espin
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
INFERRED
HumanROBO364221roundabout, axon guidance receptor, homolog 3 (Drosophila)
Click here to display 76 evidence detail records.
HumanLRRC464101leucine rich repeat containing 4
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004738abnormal auditory brainstem response0self