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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vestibular system physiology
Debug Stats
  • ### Total Build Time: 172 ms 21.350 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 402 bytes
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  • CONCEPT_GENES gt=75 ms Completed: 75 ms rowSize= 15.104 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal vestibular system physiology MP:0004742
Definition (1)
any functional anomaly of the sensory system responsible for the sense of head position and movement of the body through space; such anomalies may result in impaired balance, dizziness, poor regulation of postural muscle tone and inability to detect quick movements of the head
Parents (1)
img abnormal ear physiology MP:0003878
Children (4)
img abnormal linear vestibular evoked potential MP:0004812
img abnormal vestibuloocular reflex MP:0004844
img abnormal vestibulocollic reflex MP:0006377
img abnormal vestibular evoked myogenic potential MP:0004743
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053774img abnormal ear physiology MP:0003878
Genes (47)

Species:
human : 47
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Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
Click here to display 32 evidence detail records.
HumanTMIE259236transmembrane inner ear
INFERRED
HumanOTOP1133060otopetrin 1
Click here to display 32 evidence detail records.
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
INFERRED
HumanSLITRK684189SLIT and NTRK-like family, member 6
INFERRED
HumanSLC4A1183959solute carrier family 4, sodium borate transporter, member 11
INFERRED
HumanESPN83715espin
Click here to display 32 evidence detail records.
HumanTMPRSS364699transmembrane protease, serine 3
Click here to display 32 evidence detail records.
HumanROBO364221roundabout, axon guidance receptor, homolog 3 (Drosophila)
INFERRED
HumanCDH2364072cadherin-related 23
Click here to display 32 evidence detail records.
HumanBLOC1S563915biogenesis of lysosomal organelles complex-1, subunit 5, muted
INFERRED
HumanSPTBN457731spectrin, beta, non-erythrocytic 4
INFERRED
HumanSLC12A557468solute carrier family 12 (potassium/chloride transporter), member 5
INFERRED
HumanHR55806hair growth associated
INFERRED
HumanSOBP55084sine oculis binding protein homolog (Drosophila)
INFERRED
HumanMYO15A51168myosin XVA
Click here to display 32 evidence detail records.
HumanNOX350508NADPH oxidase 3
INFERRED
HumanBLOC1S626258biogenesis of lysosomal organelles complex-1, subunit 6, pallidin
INFERRED
HumanQKI9444QKI, KH domain containing, RNA binding
INFERRED
HumanS1PR29294sphingosine-1-phosphate receptor 2
Click here to display 32 evidence detail records.
HumanAP3D18943adaptor-related protein complex 3, delta 1 subunit
INFERRED
HumanNR4A38013nuclear receptor subfamily 4, group A, member 3
Click here to display 32 evidence detail records.
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED
HumanSLC30A47782solute carrier family 30 (zinc transporter), member 4
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004742abnormal vestibular system physiology0self