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Details
Link-It Detail - Jax Mouse Phenotype - abnormal spiral ligament morphology
Debug Stats
  • ### Total Build Time: 25 ms 19.767 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 398 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 313 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 199 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=4 ms Completed: 4 ms rowSize= 1.026 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.489 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.271 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 10.774 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.173 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal spiral ligament morphology MP:0004288
Definition (1)
any structural anomaly in the thickened periosteal lining of the bony cochlea that forms the outer wall of the cochlear duct to which the basal lamina attaches
Synonyms (1)
"abnormal spiral ligament of cochlear duct" EXACT
Parents (2)
img abnormal ligament morphology MP:0005504
img abnormal scala media morphology MP:0003169
Children (3)
img spiral ligament degeneration MP:0004864
img thin spiral ligament MP:0004863
img abnormal spiral ligament fibrocyte morphology MP:0004292
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053905img abnormal ligament morphology MP:0005504
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 (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanOTOS150677otospiralin
INFERRED
HumanSLC4A1183959solute carrier family 4, sodium borate transporter, member 11
INFERRED
HumanSLC12A69990solute carrier family 12 (potassium/chloride transporter), member 6
INFERRED
HumanSLC4A79497solute carrier family 4, sodium bicarbonate cotransporter, member 7
img Jax MP, Pubmed Id: 17712420, MOUSE PHENOTYPE ID: MGI:1351641
img Jax MP, Pubmed Id: 12808454, MOUSE PHENOTYPE ID: MGI:2443878
HumanTHRB7068thyroid hormone receptor, beta
INFERRED
HumanSLC12A26558solute carrier family 12 (sodium/potassium/chloride transporter), member 2
INFERRED
HumanPOU3F45456POU class 3 homeobox 4
INFERRED
HumanSLC26A45172solute carrier family 26 (anion exchanger), member 4
INFERRED
HumanNDP4693Norrie disease (pseudoglioma)
INFERRED
HumanNAGLU4669N-acetylglucosaminidase, alpha
img Jax MP, Pubmed Id: 12808454, MOUSE PHENOTYPE ID: MGI:2443878
img Jax MP, Pubmed Id: 17712420, MOUSE PHENOTYPE ID: MGI:1351641
HumanMAN2B14125mannosidase, alpha, class 2B, member 1
INFERRED
HumanIDUA3425iduronidase, alpha-L-
INFERRED
HumanGRID12894glutamate receptor, ionotropic, delta 1
INFERRED
HumanGABRB32562gamma-aminobutyric acid (GABA) A receptor, beta 3
INFERRED
HumanGABRB22561gamma-aminobutyric acid (GABA) A receptor, beta 2
INFERRED
HumanGABRA52558gamma-aminobutyric acid (GABA) A receptor, alpha 5
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004288abnormal spiral ligament morphology0self