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Details
Link-It Detail - Jax Mouse Phenotype - small basisphenoid bone
Debug Stats
  • ### Total Build Time: 20 ms 16.845 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 374 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 467 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 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=3 ms Completed: 3 ms rowSize= 592 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 585 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 5.615 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 7.953 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.161 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
small basisphenoid bone MP:0004462
Definition (1)
reduced size 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
Parents (1)
img abnormal basisphenoid bone morphology MP:0000106
Children (1)
img basisphenoid bone hypoplasia MP:0004461
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053828img abnormal basisphenoid bone morphology MP:0000106
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053909img abnormal basisphenoid bone morphology MP:0000106
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053829img abnormal basisphenoid bone morphology MP:0000106
img mammalian phenotype MP:0000001img skeleton phenotype MP:000539010img abnormal basisphenoid bone morphology MP:0000106
Genes (13)

Species:
human : 13
SpeciesGeneGeneIdGene NameEvidence
HumanTMEM10784314transmembrane protein 107
Click here to display 19 evidence detail records.
HumanFGFRL153834fibroblast growth factor receptor-like 1
Click here to display 19 evidence detail records.
HumanCDON50937cell adhesion associated, oncogene regulated
Click here to display 19 evidence detail records.
HumanWNT17471wingless-type MMTV integration site family, member 1
Click here to display 19 evidence detail records.
HumanSKI6497v-ski avian sarcoma viral oncogene homolog
Click here to display 19 evidence detail records.
HumanMN14330meningioma (disrupted in balanced translocation) 1
INFERRED
HumanLTBP14052latent transforming growth factor beta binding protein 1
Click here to display 19 evidence detail records.
HumanGLI32737GLI family zinc finger 3
Click here to display 19 evidence detail records.
HumanFOXC22303forkhead box C2 (MFH-1, mesenchyme forkhead 1)
Click here to display 19 evidence detail records.
HumanFOXC12296forkhead box C1
Click here to display 19 evidence detail records.
HumanRUNX2860runt-related transcription factor 2
Click here to display 19 evidence detail records.
HumanBMP7655bone morphogenetic protein 7
Click here to display 19 evidence detail records.
HumanNKX3-2579
Click here to display 19 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004462small basisphenoid bone0self