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Details
Link-It Detail - Jax Mouse Phenotype - abnormal endolymph
Debug Stats
  • ### Total Build Time: 37 ms 22.782 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 364 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 453 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 182 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=2 ms Completed: 2 ms rowSize= 578 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.938 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.577 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 16.426 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.156 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal endolymph MP:0004885
Definition (1)
any alteration in the normal production (volume) or ionic homeostasis of the fluid contained within the membranous labyrinth of the inner ear; unlike perilymph, endolymph resembles intracellular fluid in composition and has a high concentration of potassium ion and a low concentration of sodium ion
Synonyms (1)
"abnormal Scarpa's liquor" EXACT
Parents (1)
img abnormal ear physiology MP:0003878
Children (4)
img abnormal vestibular endolymph MP:0006389
img abnormal cochlear endolymph MP:0006390
img decreased endolymph production MP:0004887
img increased endolymph production MP:0004886
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053774img abnormal ear physiology MP:0003878
Genes (22)

Species:
human : 22
SpeciesGeneGeneIdGene NameEvidence
HumanSLC4A1183959solute carrier family 4, sodium borate transporter, member 11
INFERRED
HumanESPN83715espin
INFERRED
HumanFBXO1180204F-box protein 11
INFERRED
HumanATP6V0A450617ATPase, H+ transporting, lysosomal V0 subunit a4
INFERRED
HumanGJB610804gap junction protein, beta 6, 30kDa
INFERRED
HumanSLC12A69990solute carrier family 12 (potassium/chloride transporter), member 6
INFERRED
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED
HumanTYRP17306tyrosinase-related protein 1
INFERRED
HumanTHRA7067thyroid hormone receptor, alpha
INFERRED
HumanPOU3F45456POU class 3 homeobox 4
INFERRED
HumanSLC26A45172solute carrier family 26 (anion exchanger), member 4
INFERRED
HumanCLDN115010claudin 11
INFERRED
HumanNEUROD14760neuronal differentiation 1
INFERRED
HumanKIT3815v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
INFERRED
HumanKCNJ103766potassium inwardly-rectifying channel, subfamily J, member 10
INFERRED
HumanGRID12894glutamate receptor, ionotropic, delta 1
INFERRED
HumanFOXI12299forkhead box I1
INFERRED
HumanFGFR12260fibroblast growth factor receptor 1
INFERRED
HumanESRRB2103estrogen-related receptor beta
INFERRED
HumanEPHB32049EPH receptor B3
img Jax MP, Pubmed Id: 17158005, MOUSE PHENOTYPE ID: MGI:104770
img Jax MP, Pubmed Id: 17158005, MOUSE PHENOTYPE ID: MGI:104770
img Jax MP, Pubmed Id: 17158005, MOUSE PHENOTYPE ID: MGI:105097
img Jax MP, Pubmed Id: 17158005, MOUSE PHENOTYPE ID: MGI:105097
HumanEFNB21948ephrin-B2
img Jax MP, Pubmed Id: 17158005, MOUSE PHENOTYPE ID: MGI:104770
img Jax MP, Pubmed Id: 17158005, MOUSE PHENOTYPE ID: MGI:104770
img Jax MP, Pubmed Id: 17158005, MOUSE PHENOTYPE ID: MGI:105097
img Jax MP, Pubmed Id: 17158005, MOUSE PHENOTYPE ID: MGI:105097
HumanSCARB2950scavenger receptor class B, member 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004885abnormal endolymph0self