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Details
Link-It Detail - Jax Mouse Phenotype - abnormal basisphenoid bone morphology
Debug Stats
  • ### Total Build Time: 82 ms 26.932 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 402 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 477 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 185 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=1 ms Completed: 1 ms rowSize= 1.031 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 2.408 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 5.595 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=78 ms Completed: 78 ms rowSize= 15.539 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal basisphenoid bone morphology MP:0000106
Definition (1)
any structural anomaly of part of the base of the cranium between the basioccipital and the presphenoid, which usually ossifies separately in the embryo or in the young, and becomes a part of the sphenoid in the adult; in many animals it persists as a separate bone between the basioccipital bone and the presphenoidal bone
Synonyms (1)
"basisphenoid bone dysplasia" EXACT
Parents (2)
img abnormal basicranium morphology MP:0010029
img abnormal sphenoid bone morphology MP:0000104
Children (5)
img absent basisphenoid bone MP:0008385
img impaired ossification of basisphenoid bone MP:0000105
img small basisphenoid bone MP:0004462
img fusion of basioccipital and basisphenoid bone MP:0004572
img basisphenoid bone foramen MP:0004463
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053827img abnormal basicranium morphology MP:0010029
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053908img abnormal basicranium morphology MP:0010029
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
Genes (38)

Species:
human : 38
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanBMPER168667BMP binding endothelial regulator
Click here to display 34 evidence detail records.
HumanPKDCC91461protein kinase domain containing, cytoplasmic
INFERRED
HumanDISP184976dispatched homolog 1 (Drosophila)
Click here to display 34 evidence detail records.
HumanTMEM10784314transmembrane protein 107
INFERRED
HumanSULF255959sulfatase 2
Click here to display 34 evidence detail records.
HumanFGFRL153834fibroblast growth factor receptor-like 1
INFERRED
HumanCDON50937cell adhesion associated, oncogene regulated
INFERRED
HumanKIF3A11127kinesin family member 3A
Click here to display 34 evidence detail records.
HumanCHRD8646chordin
INFERRED
HumanALX18092ALX homeobox 1
Click here to display 34 evidence detail records.
HumanWNT17471wingless-type MMTV integration site family, member 1
INFERRED
HumanZEB16935zinc finger E-box binding homeobox 1
Click here to display 34 evidence detail records.
HumanTBX16899T-box 1
INFERRED
HumanSP36670Sp3 transcription factor
Click here to display 34 evidence detail records.
HumanSMO6608smoothened, frizzled family receptor
Click here to display 34 evidence detail records.
HumanSKI6497v-ski avian sarcoma viral oncogene homolog
INFERRED
HumanPDGFRA5156platelet-derived growth factor receptor, alpha polypeptide
INFERRED
HumanOTX25015orthodenticle homeobox 2
Click here to display 34 evidence detail records.
HumanOTX15013orthodenticle homeobox 1
INFERRED
HumanMN14330meningioma (disrupted in balanced translocation) 1
INFERRED
HumanLTBP14052latent transforming growth factor beta binding protein 1
INFERRED
HumanHOXA23199homeobox A2
Click here to display 34 evidence detail records.
HumanGLI32737GLI family zinc finger 3
Click here to display 34 evidence detail records.
HumanGLI22736GLI family zinc finger 2
Click here to display 34 evidence detail records.
HumanFOXC22303forkhead box C2 (MFH-1, mesenchyme forkhead 1)
Click here to display 34 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000106abnormal basisphenoid bone morphology0self