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Details
Link-It Detail - Jax Mouse Phenotype - abnormal stria vascularis morphology
Debug Stats
  • ### Total Build Time: 48 ms 24.723 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 400 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 642 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 212 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 2.894 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.936 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=37 ms Completed: 37 ms rowSize= 15.778 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.174 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal stria vascularis morphology MP:0000048
Definition (1)
any structural anomaly in the stratified, secretory epithelium which lines the upper part of the cochlear spiral ligament and maintains potassium ion homeostasis in the endolymph; stria vascularis normally consists of marginal, intermediate, and basal cells: basal and marginal cell tight junctions preclude paracellular diffusion into and out of the intrastrial space while basal and intermediate cells secrete into this space potassium ions derived from fibrocytes through gap junctions
Synonyms (1)
"abnormal stria vascularis ductus cochlearis morphology" EXACT
Parents (1)
img abnormal scala media morphology MP:0003169
Children (6)
img abnormal strial intermediate cell morphology MP:0004367
img abnormal strial basal cell morphology MP:0004365
img abnormal stria vascularis vasculature morphology MP:0004368
img stria vascularis degeneration MP:0004363
img abnormal strial marginal cell morphology MP:0004366
img thin stria vascularis MP:0004364
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053777img abnormal scala media morphology MP:0003169
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053778img abnormal scala media morphology MP:0003169
Genes (33)

Species:
human : 33
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
Click here to display 37 evidence detail records.
HumanTSPAN1223554tetraspanin 12
INFERRED
HumanGJB610804gap junction protein, beta 6, 30kDa
Click here to display 37 evidence detail records.
HumanSLC4A79497solute carrier family 4, sodium bicarbonate cotransporter, member 7
Click here to display 37 evidence detail records.
HumanS1PR29294sphingosine-1-phosphate receptor 2
Click here to display 37 evidence detail records.
HumanAP3D18943adaptor-related protein complex 3, delta 1 subunit
Click here to display 37 evidence detail records.
HumanFZD48322frizzled family receptor 4
Click here to display 37 evidence detail records.
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
Click here to display 37 evidence detail records.
HumanTYRP17306tyrosinase-related protein 1
Click here to display 37 evidence detail records.
HumanSOD16647superoxide dismutase 1, soluble
INFERRED
HumanSLC12A26558solute carrier family 12 (sodium/potassium/chloride transporter), member 2
Click here to display 37 evidence detail records.
HumanPOU4F35459POU class 4 homeobox 3
INFERRED
HumanPOLG5428polymerase (DNA directed), gamma
INFERRED
HumanSLC26A45172solute carrier family 26 (anion exchanger), member 4
INFERRED
HumanPAX25076paired box 2
Click here to display 37 evidence detail records.
HumanCLDN115010claudin 11
Click here to display 37 evidence detail records.
HumanNDP4693Norrie disease (pseudoglioma)
INFERRED
HumanMYO7A4647myosin VIIA
INFERRED
HumanMYO64646myosin VI
INFERRED
HumanMITF4286microphthalmia-associated transcription factor
Click here to display 37 evidence detail records.
HumanLRP24036low density lipoprotein receptor-related protein 2
INFERRED
HumanLAMA23908laminin, alpha 2
INFERRED
HumanKIT3815v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
Click here to display 37 evidence detail records.
HumanKCNQ13784potassium voltage-gated channel, KQT-like subfamily, member 1
Click here to display 37 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000048abnormal stria vascularis morphology0self