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Details
Link-It Detail - Jax Mouse Phenotype - abnormal orbitosphenoid bone morphology
Debug Stats
  • ### Total Build Time: 14 ms 28.251 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 406 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 345 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=3 ms Completed: 3 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 1.025 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 588 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 6.917 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 17.485 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.177 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal orbitosphenoid bone morphology MP:0004457
Definition (1)
any structural anomaly of the bone that is situated in the orbit on either side of the presphenoid; it generally forms a part of the sphenoid in the adult, and may be independent in the young
Synonyms (1)
"abnormal lesser wing of the sphenoid bone" EXACT
Parents (2)
img abnormal sphenoid bone morphology MP:0000104
img abnormal orbit morphology MP:0010030
Children (1)
img abnormal optic canal morphology MP:0010704
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053828img abnormal sphenoid bone morphology MP:0000104
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053909img abnormal sphenoid bone morphology MP:0000104
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053827img abnormal orbit morphology MP:0010030
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053908img abnormal orbit morphology MP:0010030
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053915img abnormal orbit morphology MP:0010030
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanSMO6608smoothened, frizzled family receptor
img Jax MP, Pubmed Id: 15107405, MOUSE PHENOTYPE ID: MGI:108075
img Jax MP, Pubmed Id: 6049666, MOUSE PHENOTYPE ID: MGI:95729
img Jax MP, Pubmed Id: 9077465, MOUSE PHENOTYPE ID: MGI:97450
img Jax MP, Pubmed Id: 9077465, MOUSE PHENOTYPE ID: MGI:97450
img Jax MP, Pubmed Id: 7590242, MOUSE PHENOTYPE ID: MGI:97451
HumanRARG5916retinoic acid receptor, gamma
INFERRED
HumanRARB5915retinoic acid receptor, beta
INFERRED
HumanOTX25015orthodenticle homeobox 2
img Jax MP, Pubmed Id: 7590242, MOUSE PHENOTYPE ID: MGI:97451
img Jax MP, Pubmed Id: 15107405, MOUSE PHENOTYPE ID: MGI:108075
img Jax MP, Pubmed Id: 9077465, MOUSE PHENOTYPE ID: MGI:97450
img Jax MP, Pubmed Id: 9077465, MOUSE PHENOTYPE ID: MGI:97450
img Jax MP, Pubmed Id: 6049666, MOUSE PHENOTYPE ID: MGI:95729
HumanOTX15013orthodenticle homeobox 1
img Jax MP, Pubmed Id: 6049666, MOUSE PHENOTYPE ID: MGI:95729
img Jax MP, Pubmed Id: 7590242, MOUSE PHENOTYPE ID: MGI:97451
img Jax MP, Pubmed Id: 9077465, MOUSE PHENOTYPE ID: MGI:97450
img Jax MP, Pubmed Id: 15107405, MOUSE PHENOTYPE ID: MGI:108075
img Jax MP, Pubmed Id: 9077465, MOUSE PHENOTYPE ID: MGI:97450
HumanGLI32737GLI family zinc finger 3
img Jax MP, Pubmed Id: 6049666, MOUSE PHENOTYPE ID: MGI:95729
img Jax MP, Pubmed Id: 9077465, MOUSE PHENOTYPE ID: MGI:97450
img Jax MP, Pubmed Id: 15107405, MOUSE PHENOTYPE ID: MGI:108075
img Jax MP, Pubmed Id: 7590242, MOUSE PHENOTYPE ID: MGI:97451
img Jax MP, Pubmed Id: 9077465, MOUSE PHENOTYPE ID: MGI:97450
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004457abnormal orbitosphenoid bone morphology0self