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Details
Link-It Detail - Jax Mouse Phenotype - abnormal basilar membrane morphology
Debug Stats
  • ### Total Build Time: 22 ms 14.787 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= 410 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 211 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=10 ms Completed: 10 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.581 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 10.314 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 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 basilar membrane morphology MP:0004308
Definition (1)
any structural anomaly in the membrane extending from the bony spiral membrane to the basilar crest of the cochlea; it forms the greater part of the floor of the cochlear duct separating the latter from the scala tympani, and it supports the organ of Corti
Synonyms (1)
"abnormal basilar membrane of cochlear duct morphology" EXACT
Parents (1)
img abnormal cochlea morphology MP:0000031
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053776img abnormal cochlea morphology MP:0000031
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanPOU4F35459POU class 4 homeobox 3
img Jax MP, Pubmed Id: 16051453, MOUSE PHENOTYPE ID: MGI:88057
img Jax MP, Pubmed Id: 15891643, MOUSE PHENOTYPE ID: MGI:108083
img Jax MP, Pubmed Id: 10452377, MOUSE PHENOTYPE ID: MGI:102523
img Jax MP, Pubmed Id: 21179397, MOUSE PHENOTYPE ID: MGI:1933750
HumanKCNQ13784potassium voltage-gated channel, KQT-like subfamily, member 1
img Jax MP, Pubmed Id: 10452377, MOUSE PHENOTYPE ID: MGI:102523
img Jax MP, Pubmed Id: 16051453, MOUSE PHENOTYPE ID: MGI:88057
img Jax MP, Pubmed Id: 21179397, MOUSE PHENOTYPE ID: MGI:1933750
img Jax MP, Pubmed Id: 15891643, MOUSE PHENOTYPE ID: MGI:108083
HumanAPOE348apolipoprotein E
img Jax MP, Pubmed Id: 21179397, MOUSE PHENOTYPE ID: MGI:1933750
img Jax MP, Pubmed Id: 10452377, MOUSE PHENOTYPE ID: MGI:102523
img Jax MP, Pubmed Id: 16051453, MOUSE PHENOTYPE ID: MGI:88057
img Jax MP, Pubmed Id: 15891643, MOUSE PHENOTYPE ID: MGI:108083
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004308abnormal basilar membrane morphology0self